Inguinal and Ventral Hernia Repair by Sublay, Underlay and IPOM Mesh FixationAGluTHeMFixNCT06462066
Effectiveness, Appropriateness and Safety of GLUTACK-Glubran Tiss 2 Surgical Glue Compared to GLUTACK-Glubran 2 Device System for Mesh Fastening in Laparoscopic and Robotic Hernia Surgery
A study testing Experimental medical device and Comparator medical device in people with Inguinal and Ventral Hernia Repair by Sublay, Underlay and IPOM Mesh Fixation, run by GEM SRL at 1 site in Italy.
Trial summary
This pre-market, prospective, randomized, non-inferiority clinical study was designed to evaluate the safety and performance/effectiveness of Glutack-Glubran® Tiss 2 system compared to Glutack-Glubran® used for mesh fixation in laparoscopic and robotic hernia surgery to obtain the indication and upgrade the medical… Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Inguinal and Ventral Hernia Repair by Sublay, Underlay and IPOM Mesh Fixation
- What is being tested?
- Experimental medical device and Comparator medical device
- Type of treatment
- Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 101 participants
- Where
- 1 siteItaly
- Study dates
- 19 Oct 2020to 29 Jun 2023
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- No significant cardiopulmonary, hepatic, or renal impairment, and no contraindications for surgery;
- Clinical diagnosis of:
- bilateral inguinal hernia eligible for minimally invasive repair (TAPP-TEP VLS/ROB)
- recurrent monoliteral inguinal hernia (TAPP-TEP VLS/ROB)
- large inguinoscrotal hernias (TAPP-TEP ROB)
- primary ventral hernia with defects size ≤ 7cm (IPOM-TARUP-COSTA-THT-MILOS-eMILOS VLS/ROB)
Show all 14Show fewer
- primary abdominal border hernia (idem VLS/ROB)
- post-incisional hernia with defect size ≤ 7cm (idem VLS)
- post-incisional hernia and complex abdomen (RIVES-RIVES+TAR ROB)
- swiss-cheese defects multiple small defects if treatable with only one mesh; if the total width of the defect is ≤ 5cm will be repaired by IPOM VLSM; if it is > 5cm will be repaired by RIVES-RIVES+TAR ROB;
- Age > 18 years, male and female;
- Obese patient (BMI>35);
- Patients with ASA grade from I to III;
- Patients must sign and date the informed consent form prior to treatment.
Who cannot join
- Incarcerated hernia;
- Allergy to multiple classes of drugs, recent allergic disease, or use of drugs that are known harmful to vital organs during the 4 weeks before surgery;
- Patients with ASA IV or V;
- Participations in other clinical studies in the 3 months before surgery;
- Atopic allergy history;
- Mental illness history;
Show all 13Show fewer
- Diseases that may significantly increase Intra-Abdominal Pressure (IAP) and cannot be effectively controlled such as severe ascites, severe asthma caused by bronchitis, pulmonary emphysema, or urine retention caused by significant Benign Prostatic Hyperplasia (BPH);
- Infection located at the surgical site or bacteraemia;
- Patients with collagenopathies;
- Relevant other concurrent diseases;
- Patient with neurological disorders and/or mood disorders;
- Hyperemotional patients;
- Pregnant women.
Trial locations and contacts
1 site in 1 country.
Italy1 site
Ospedale Misericordia - U.O.C Chirurgia Generale e Mini-Invasiva.
Grosseto, 58100
About this study
Official title: Effectiveness, Appropriateness and Safety of GLUTACK-Glubran® Tiss 2 Surgical Glue (NBCA: n Butyl 2 Cyanoacrylate + OCA: 2-Octyl-Cyanoacrylate) Compared to GLUTACK-Glubran® 2 Device System for Mesh Fastening in Laparoscopic and Robotic Hernia Surgery (Inguinal and Ventral Hernia Repair by Sublay, Underlay and IPOM Mesh Fixation).
This pre-market, prospective, randomized, non-inferiority clinical study was designed to evaluate the safety and performance/effectiveness of Glutack-Glubran® Tiss 2 system compared to Glutack-Glubran® used for mesh fixation in laparoscopic and robotic hernia surgery to obtain the indication and upgrade the medical device Glubran® Tiss 2 to class IIb.Cyanoacrylate is the generic name of a group of fast-acting adhesives such as ethyl-2-cyanoacrylate, n-butyl cyanoacrylate, 2-octy1 cyanoacrylate sold under various trade names and blend. Cyanoacrylate is a liquid acrylate monomer that polymerizes exothermically in the presence of water, especially with hydroxide ions, joining the bonded surfaces in 4-5 s and reaching the final stage in 60-90 s . It bonds body tissue excellently and shows bacteriostatic effects . The film of glue is eliminated by hydrolytic breakdown, a process whose duration varies according to tissue type and quantity .
In contrast to most cyanoacrylate glues used only for external applications as skin wound closure, Glubran® 2 is a modified n-butyl-cyanoacrylate (Glubran® 2 - N-Butyl 2 Cyanoaciylate [NBCA]+ Methacryloxysulfolane [MS]), class III medical device, CE-certified for both external and internal use .
Read more
Glubran® 2 effectiveness in repairing hernias with less post-operative pain, less complications, less hernia recurrences and a greater cost-effectiveness is largely documented . Other cyanoacrylate-based glues are authorized to fix hernia meshes, i.e.: Histoacryl (pure NBCA; classified as class IIb medical device), Liquibond FIX8 (pure NBCA; classified as class III medical device) and Ifabond (n-hexyl-cyanoacrylate; classified as class III medical device). Others are authorized to be used for specific internal indication like Omnex (2-Octyl-CyanoAcrylate [OCA] + Butyl-Lactoyl-Cyanoacrylate), which is indicated for use in vascular reconstructions. Sometimes, abroad, also some cyanoacrylate-based glues are applied for internal uses even if not authorized .
The present prospective and randomized study was aimed at comparing the effectiveness and safety of another cyanoacrylate-based glue called Glubran® Tiss 2 (NBCA + OCA), classified as class IIa surgical medical device, CE-marked (under the European Union [EU] Directive 93/42 EEC), being already authorized for use as atraumatic fixation system: Glubran® 2. Both medical devices have previously demonstrated to be well-tolerated and safe.
Glubran® 2 and Glubran® Tiss 2 were to be applied by Glutack®, a CE-marked medical device system for glue application in the surgical field. Glutack® is the related Glubran® 2/ Glubran® Tiss 2 applicator device for laparoscopic mesh fixation procedures was fabricated to offer a precise and controlled delivery of Glubran® glues .
Glubran® Tiss 2 fulfils the requirements of EU Medical Device Regulation (MDR) 2017/745 (confirmation letter received by the relative Notified Body). The composition of Glubran® Tiss 2 is obtained by mixing two different monomers of cyanoacrylate (NBCA + OCA); this gives the product a better elasticity, while maintaining high levels of tensile strength. In fact, international scientific literature has shown that the common NBCA is the cyanoacrylate molecule with the greatest tensile strength (34.27 N), low elasticity, while OCA has a lower resistance (11.27 N) but has good elastic properties. Glubran® Tiss 2 glue has a tensile strength of 27.34 N and thanks to the presence of OCA, also excellent elasticity . Among its characteristics, this formulation has haemostatic, sealing, bacteriostatic and adhesive properties. Polymerization begins 1-2 seconds after application and completes within 60 seconds. The polymerization reaction generates a temperature of approximately 45°C, which is lower than that of pure cyanoacrylates .
Glubran® Tiss 2, indicated also for use in paediatrics, is a sterile, ready for use, blended cyanacrylate adhesive to be used on the skin and mucosal tissues, which is approved as class IIa medical device, effective even in patients anticoagulated and with congenital coagulopathies .
Read the detailed description
This was a pre-market, prospective, randomized, non-inferiority, clinical study aimed at evaluating the safety and performance/effectiveness of Glutack-Glubran® Tiss 2 system compared to Glutack-Glubran® 2 applied for mesh fastening in laparoscopic and robotic hernia surgery to get the indication and upgrade Glubran® Tiss 2 to class IIb. The study was conducted in seven centres in Italy and was to enroll 100 patients. Patients were to be followed for 6 months. The global duration of the trial was approximately 32 months.
According to the CIP, 6 Visits were planned over the perioperative/post operative period for each patient (after 24 hours,7, 14, 90, and 180 days).
At Visit 1 (V1, day 0, Baseline visit), patients were requested to sign the written informed consent before any procedure was performed. Patients were screened for eligibility for the study ascertaining that all inclusion criteria and no exclusion criteria were met. At V1, the Investigator recorded demographic and medical history, basal clinical assessment data and performed full physical examination and evaluation of clinical signs/symptoms.
Patients were randomly assigned (1:1 allocation ratio) to one of the two treatment groups: Glutack-Glubran® system (Group 1) or Glutack-Glubran® Tiss 2 (Group 2). The application of Glutack-Glubran® system or Glutack-Glubran® Tiss 2 was performed by the investigator, after a previous appropriate training on how to assemble/use each device.
Technical success of glue fastening was evaluated intra-operatively, the investigator registered whether mesh fixation system achieved technical success or not. Technical success was to be defined as successful hernia repair as intended, but actually defined in the present analysis as a surgical procedure with no complications within the first 24 hours after surgery and a surgeon's rating for Efficacy and Control greater than or equal to 4.At specific intervals, at V2 (24 hours), V3 (7 days), V4 (14 days), V5 (90 days) and V6 (180 days), patients were requested to return to the centre for the clinical assessments of safety, quality of life and effectiveness. As regards effectiveness, at each Visit, the area of the mesh implant was evaluated for recurrence through a specific abdominal clinical examination. In case of any suspicion of recurrence, an ultrasound or MRI was to be performed according to hospital practice to distinguish true hernia recurrences from bulging. At V6 cost effectiveness was also to be evaluated.The primary objective of the study was to assess the effectiveness of Glutack-Glubran® Tiss 2 mesh fastening in comparison with mesh fixation by Glutack-Glubran® 2 evaluated in terms of hernia recurrence rate after surgery and technical success of glue fastening (evaluated intra-operatively).
The secondary objectives were aimed at investigating the following:
- Safety in terms of side effects
- Cost effectiveness in terms of direct costs of intervention, operating and hospitalization times, times of return to normal activity
- The adequacy of Glutack® medical device for the application of surgical glue for fixing the prosthesis (mesh) in terms of ease of use and satisfaction of the surgeon.
This study enrolled 107 adult patients submitted to surgical treatment for laparoceles (incisional hernia) or monolateral or bilateral inguinal hernia.
6.3.1 Inclusion Criteria
Patients could be enrolled in the investigation if they met all the following inclusion criteria:
- No significant cardiopulmonary, hepatic, or renal impairment, and no contraindications for surgery;
- Clinical diagnosis of:
- bilateral inguinal hernia eligible for minimally invasive repair (TAPP-TEP VLS/ROB)
- recurrent monoliteral inguinal hernia (TAPP-TEP VLS/ROB)
- large inguinoscrotal hernias (TAPP-TEP ROB)
- primary ventral hernia with defects size ≤ 7cm (IPOM-TARUP-COSTA-THT-MILOS-eMILOS VLS/ROB)
- primary abdominal border hernia (idem VLS/ROB)
- post-incisional hernia with defect size ≤ 7cm (idem VLS)
- post-incisional hernia and complex abdomen (RIVES-RIVES+TAR ROB)
- Swiss-cheese defects multiple small defects if treatable with only one mesh; if the total width of the defect is ≤ 5cm will be repaired by IPOM VLSM; if it is > 5cm will be repaired by RIVES-RIVES+TAR ROB;
- Age > 18 years, male and Female;
- Obese patient (BMI>35);
- Patients with ASA grade from I to III;
- Patients must sign and date the informed consent form prior to treatment. 6.3.2 Exclusion Criteria
Patients could not be enrolled in the investigation if they met any of the following exclusion criteria:
- Incarcerated hernia;
- Allergy to multiple classes of drugs, recent allergic disease, or use of drugs that are known harmful to vital organs during the 4 weeks before surgery;
- Patients with ASA IV or V;
- Participations in other clinical studies in the 3 months before surgery;
- Atopic allergy history;
- Mental illness history;
- Diseases that may significantly increase Intra-Abdominal Pressure (IAP) and cannot be effectively controlled such as severe ascites, severe asthma caused by bronchitis, pulmonary emphysema, or urine retention caused by significant Benign Prostatic Hyperplasia (BPH);
- Infection located at the surgical site or bacteraemia;
- Patients with collagenopathies;
- Relevant other concurrent diseases;
- Patient with neurological disorders and/or mood disorders;
- Hyperemotional patients;
- Pregnant women.
- Being tested
- Experimental medical device, Comparator medical device
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Experimental medical deviceProcedure or surgery
Also called Glubran Tiss
Open the blister and pour the sterile single-dose bottle onto the operating table in a sterile field. Before opening the single-dose bottle verify the state of fluidity of the glue and its transparency. Open the single dose of Gluban Tiss® 2. Insert the transfer tip on the single dose, grabbing it near the neck to apply adequate pressure that allows the insertion of the tip. Gradually fill the cartridge by carefully pressing on the body of the single dose.
Comparator medical deviceProcedure or surgery
Also called Glubran 2
Open the blister and pour the sterile single-dose bottle onto the operating table in a sterile field. Before opening the single-dose bottle verify the state of fluidity of the glue and its transparency. Open the single dose of Glubran® 2. Insert the transfer tip on the single dose, grabbing it near the neck to apply adequate pressure that allows the insertion of the tip. Gradually fill the cartridge by carefully pressing on the body of the single dose.
| Study group | Role | What they receive |
|---|---|---|
| Glubran® Tiss | Experimental | The application of treatment will be performed by the Investigator that will be instructed for the application of Glutack/Glubran® Tiss 2 system.
Glutack® is a user-friendly device for the atraumatic laparoscopic fixation of hernia mesh. Providing precise and consistent delivery of Glubran® Tiss 2/Glubran® 2 with every pull of the trigger, to minimize surgical complications and the potential pain associated with the use of tacks and staples. Receives: Procedure: Experimental medical device |
| Glubran® 2 | Active comparator | The application of treatment will be performed by the Investigator that will be instructed for the application of Glutack/Glubran® 2 system.
Glutack® is a user-friendly device for the atraumatic laparoscopic fixation of hernia mesh. Providing precise and consistent delivery of Glubran® Tiss 2/Glubran® 2 with every pull of the trigger, to minimize surgical complications and the potential pain associated with the use of tacks and staples. Receives: Procedure: Comparator medical device |
What is being measured
The primary outcome is the main question the study is designed to answer.
Effectiveness
A clinical examination will be conducted to evaluate recurrence. If there will be any suspicion of recurrence, an ultrasound, MRI or CT is performed according to hospital practice to distinguish true hernia recurrences from bulging. Technical success of glue fastening will be evaluated intra-operatively, the investigator will register whether mesh fixation system achieved technical success or not. Technical success is defined as successful hernia repair as intended.
Measured: Verification of hernia recurrence at 1 day, 1 or 2 weeks, 3 months, 6 months
Secondary outcomes (5)
Clinical Safety:
Percentage assessment of adverse effects and events like postoperative complications including wound infection, local hematoma formation, seroma, pain, chronic pain.
Measured: Verification of Clinical safety at 1 day, 1 or 2 weeks, 3 months, 6 months
Chronic pain
Chronic pain, will be defined as moderate or greater pain in the inguinal area 3 months after surgery in which the VAS pain score was ≥4. For the evaluation of pain, an analogical visual scale will be used, identical both for the pre-operative period and for subsequent monitoring timetable. VAS pain score will be determined based on a scale of 0-10 with 0 equal to no pain and 10 equal to the worse pain imaginable.
Measured: Verification of chronic pain at 3 months, 6 months
Quality of the life
Assessed by the EuraHS-QoL score. It is a method to measure the quality of life for patients before (preoperative) and after (post=operative) an operation of an abdominal wall hernia with or without an implantation of a mesh to repair the defect. It is a questionnaire developed by the Working Group of the European Registry for Abdominal Wall Hernias (EuraHS). The EuraHS-QoL score is based on a Numerical Rating Scale for three dimensions:
- pain at the site of the hernia or the hernia repair;
- restriction of activities;
- cosmetic discomfort;
Measured: Verification of QoL at 1 day, 1 or 2 weeks, 3 months, 6 months
Cost effectiveness
Operating time, postoperative duration of stay, hospital costs, times to ambulatory visits, re-hospitalization for severe complications, Period to return to normal activity, measured in term of number of days after the index-procedure at which the patient resumes normal activities.
Measured: Verification of cost effectiveness at 1 day, 1 or 2 weeks, 3 months, 6 months
Appropriateness
Appropriateness of the glue fixation system for prosthetic fixing (mesh) GLUTACK-Glubran® Tiss 2 and Glubran® assessed by the technical success of fixing the product, evaluated intra-operatively. The investigator will record if the glue fixation system for fixing the prosthesis (mesh) GLUTACK has achieved technical success or not. "Proper Use" is defined as the successful completion of all the following five steps:
- Attaching the cannula to handle properly;
- Positioning correctly the GLUTACK® device for procedure as per the user manual's instructions;
- Using the device's control button correctly for suitable application;
- Placing the cannula tip correctly at the surgical opening;
- Using the device for up to but not exceeding 60 seconds.
Measured: Verification of Appropriateness at Intervention day during the procedure
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted17 Jun 2024
- Study start19 Oct 2020
- Primary completion29 Jun 2023
- Study completion29 Jun 2023
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Inguinal and Ventral Hernia Repair by Sublay, Underlay and IPOM Mesh FixationStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- The study plan will include a baseline visit (V1), in which eligible patients will be randomly assigned in one of the two groups: Group 1 will apply GLUTACK/Glubran® Tiss 2 whereas Group 2 GLUTACK-Glubran® 2. Application of surgical glue will be done by the surgeons, after a previous appropriate training, carried out by principal investigator (standardization application mode). Trial parameters will be recorded by a clinical evaluator at 24 hours (V2), 7 days (V3), 14 days (V4), 90 days (V5) and 180 days (V6). The last evaluation will be performed at V6, after 6 month.
- Masking
- None (open label)
- Enrolment
- 101 participants (actual)
Sponsor and investigators
- Lead sponsor
- GEM SRL
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06462066
- Sponsor's protocol ID
- DGDMF/P/I.5.i.m.2/2019/1321
- Acronym
- AGluTHeMFix
- Status last verified
- Jun 2024
- First submitted
- 12 Jun 2024
- Last updated
- 17 Jun 2024
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 17 Jun 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effectiveness, Appropriateness and Safety of GLUTACK-Glubran® Tiss 2 Surgical Glue (NBCA: n Butyl 2 Cyanoacrylate + OCA: 2-Octyl-Cyanoacrylate) Compared to GLUTACK-Glubran® 2 Device System for Mesh Fastening in Laparoscopic and Robotic Hernia Surgery (Inguinal and Ventral Hernia Repair by Sublay, Underlay and IPOM Mesh Fixation).
- ClinicalTrials.gov ID
- NCT06462066
- Acronym / sponsor ID
- AGluTHeMFix / DGDMF/P/I.5.i.m.2/2019/1321
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 101 participants (actual)
- Lead sponsor
- GEM SRLIndustry (pharma, biotech, devices)
- Study start
- 19 Oct 2020 (actual)
- Primary completion
- 29 Jun 2023 (actual)
- Study completion
- 29 Jun 2023 (actual)
- First posted
- 17 Jun 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This pre-market, prospective, randomized, non-inferiority clinical study was designed to evaluate the safety and performance/effectiveness of Glutack-Glubran® Tiss 2 system compared to Glutack-Glubran® used for mesh fixation in laparoscopic and robotic hernia surgery to obtain the indication and upgrade the medical device Glubran® Tiss 2 to class IIb.Cyanoacrylate is the generic name of a group of fast-acting adhesives such as ethyl-2-cyanoacrylate, n-butyl cyanoacrylate, 2-octy1 cyanoacrylate sold under various trade names and blend. Cyanoacrylate is a liquid acrylate monomer that polymerizes exothermically in the presence of water, especially with hydroxide ions, joining the bonded surfaces in 4-5 s and reaching the final stage in 60-90 s . It bonds body tissue excellently and shows bacteriostatic effects . The film of glue is eliminated by hydrolytic breakdown, a process whose duration varies according to tissue type and quantity .
In contrast to most cyanoacrylate glues used only for external applications as skin wound closure, Glubran® 2 is a modified n-butyl-cyanoacrylate (Glubran® 2 - N-Butyl 2 Cyanoaciylate [NBCA]+ Methacryloxysulfolane [MS]), class III medical device, CE-certified for both external and internal use .
Glubran® 2 effectiveness in repairing hernias with less post-operative pain, less complications, less hernia recurrences and a greater cost-effectiveness is largely documented . Other cyanoacrylate-based glues are authorized to fix hernia meshes, i.e.: Histoacryl (pure NBCA; classified as class IIb medical device), Liquibond FIX8 (pure NBCA; classified as class III medical device) and Ifabond (n-hexyl-cyanoacrylate; classified as class III medical device). Others are authorized to be used for specific internal indication like Omnex (2-Octyl-CyanoAcrylate [OCA] + Butyl-Lactoyl-Cyanoacrylate), which is indicated for use in vascular reconstructions. Sometimes, abroad, also some cyanoacrylate-based glues are applied for internal uses even if not authorized .
The present prospective and randomized study was aimed at comparing the effectiveness and safety of another cyanoacrylate-based glue called Glubran® Tiss 2 (NBCA + OCA), classified as class IIa surgical medical device, CE-marked (under the European Union [EU] Directive 93/42 EEC), being already authorized for use as atraumatic fixation system: Glubran® 2. Both medical devices have previously demonstrated to be well-tolerated and safe.
Glubran® 2 and Glubran® Tiss 2 were to be applied by Glutack®, a CE-marked medical device system for glue application in the surgical field. Glutack® is the related Glubran® 2/ Glubran® Tiss 2 applicator device for laparoscopic mesh fixation procedures was fabricated to offer a precise and controlled delivery of Glubran® glues .
Glubran® Tiss 2 fulfils the requirements of EU Medical Device Regulation (MDR) 2017/745 (confirmation letter received by the relative Notified Body). The composition of Glubran® Tiss 2 is obtained by mixing two different monomers of cyanoacrylate (NBCA + OCA); this gives the product a better elasticity, while maintaining high levels of tensile strength. In fact, international scientific literature has shown that the common NBCA is the cyanoacrylate molecule with the greatest tensile strength (34.27 N), low elasticity, while OCA has a lower resistance (11.27 N) but has good elastic properties. Glubran® Tiss 2 glue has a tensile strength of 27.34 N and thanks to the presence of OCA, also excellent elasticity . Among its characteristics, this formulation has haemostatic, sealing, bacteriostatic and adhesive properties. Polymerization begins 1-2 seconds after application and completes within 60 seconds. The polymerization reaction generates a temperature of approximately 45°C, which is lower than that of pure cyanoacrylates .
Glubran® Tiss 2, indicated also for use in paediatrics, is a sterile, ready for use, blended cyanacrylate adhesive to be used on the skin and mucosal tissues, which is approved as class IIa medical device, effective even in patients anticoagulated and with congenital coagulopathies .
Detailed description
This was a pre-market, prospective, randomized, non-inferiority, clinical study aimed at evaluating the safety and performance/effectiveness of Glutack-Glubran® Tiss 2 system compared to Glutack-Glubran® 2 applied for mesh fastening in laparoscopic and robotic hernia surgery to get the indication and upgrade Glubran® Tiss 2 to class IIb. The study was conducted in seven centres in Italy and was to enroll 100 patients. Patients were to be followed for 6 months. The global duration of the trial was approximately 32 months.
According to the CIP, 6 Visits were planned over the perioperative/post operative period for each patient (after 24 hours,7, 14, 90, and 180 days).
At Visit 1 (V1, day 0, Baseline visit), patients were requested to sign the written informed consent before any procedure was performed. Patients were screened for eligibility for the study ascertaining that all inclusion criteria and no exclusion criteria were met. At V1, the Investigator recorded demographic and medical history, basal clinical assessment data and performed full physical examination and evaluation of clinical signs/symptoms.
Patients were randomly assigned (1:1 allocation ratio) to one of the two treatment groups: Glutack-Glubran® system (Group 1) or Glutack-Glubran® Tiss 2 (Group 2). The application of Glutack-Glubran® system or Glutack-Glubran® Tiss 2 was performed by the investigator, after a previous appropriate training on how to assemble/use each device.
Technical success of glue fastening was evaluated intra-operatively, the investigator registered whether mesh fixation system achieved technical success or not. Technical success was to be defined as successful hernia repair as intended, but actually defined in the present analysis as a surgical procedure with no complications within the first 24 hours after surgery and a surgeon's rating for Efficacy and Control greater than or equal to 4.At specific intervals, at V2 (24 hours), V3 (7 days), V4 (14 days), V5 (90 days) and V6 (180 days), patients were requested to return to the centre for the clinical assessments of safety, quality of life and effectiveness. As regards effectiveness, at each Visit, the area of the mesh implant was evaluated for recurrence through a specific abdominal clinical examination. In case of any suspicion of recurrence, an ultrasound or MRI was to be performed according to hospital practice to distinguish true hernia recurrences from bulging. At V6 cost effectiveness was also to be evaluated.The primary objective of the study was to assess the effectiveness of Glutack-Glubran® Tiss 2 mesh fastening in comparison with mesh fixation by Glutack-Glubran® 2 evaluated in terms of hernia recurrence rate after surgery and technical success of glue fastening (evaluated intra-operatively).
The secondary objectives were aimed at investigating the following:
- Safety in terms of side effects
- Cost effectiveness in terms of direct costs of intervention, operating and hospitalization times, times of return to normal activity
- The adequacy of Glutack® medical device for the application of surgical glue for fixing the prosthesis (mesh) in terms of ease of use and satisfaction of the surgeon.
This study enrolled 107 adult patients submitted to surgical treatment for laparoceles (incisional hernia) or monolateral or bilateral inguinal hernia.
6.3.1 Inclusion Criteria
Patients could be enrolled in the investigation if they met all the following inclusion criteria:
- No significant cardiopulmonary, hepatic, or renal impairment, and no contraindications for surgery;
- Clinical diagnosis of:
- bilateral inguinal hernia eligible for minimally invasive repair (TAPP-TEP VLS/ROB)
- recurrent monoliteral inguinal hernia (TAPP-TEP VLS/ROB)
- large inguinoscrotal hernias (TAPP-TEP ROB)
- primary ventral hernia with defects size ≤ 7cm (IPOM-TARUP-COSTA-THT-MILOS-eMILOS VLS/ROB)
- primary abdominal border hernia (idem VLS/ROB)
- post-incisional hernia with defect size ≤ 7cm (idem VLS)
- post-incisional hernia and complex abdomen (RIVES-RIVES+TAR ROB)
- Swiss-cheese defects multiple small defects if treatable with only one mesh; if the total width of the defect is ≤ 5cm will be repaired by IPOM VLSM; if it is > 5cm will be repaired by RIVES-RIVES+TAR ROB;
- Age > 18 years, male and Female;
- Obese patient (BMI>35);
- Patients with ASA grade from I to III;
- Patients must sign and date the informed consent form prior to treatment. 6.3.2 Exclusion Criteria
Patients could not be enrolled in the investigation if they met any of the following exclusion criteria:
- Incarcerated hernia;
- Allergy to multiple classes of drugs, recent allergic disease, or use of drugs that are known harmful to vital organs during the 4 weeks before surgery;
- Patients with ASA IV or V;
- Participations in other clinical studies in the 3 months before surgery;
- Atopic allergy history;
- Mental illness history;
- Diseases that may significantly increase Intra-Abdominal Pressure (IAP) and cannot be effectively controlled such as severe ascites, severe asthma caused by bronchitis, pulmonary emphysema, or urine retention caused by significant Benign Prostatic Hyperplasia (BPH);
- Infection located at the surgical site or bacteraemia;
- Patients with collagenopathies;
- Relevant other concurrent diseases;
- Patient with neurological disorders and/or mood disorders;
- Hyperemotional patients;
- Pregnant women.
Study design
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
- Model description
- The study plan will include a baseline visit (V1), in which eligible patients will be randomly assigned in one of the two groups: Group 1 will apply GLUTACK/Glubran® Tiss 2 whereas Group 2 GLUTACK-Glubran® 2. Application of surgical glue will be done by the surgeons, after a previous appropriate training, carried out by principal investigator (standardization application mode). Trial parameters will be recorded by a clinical evaluator at 24 hours (V2), 7 days (V3), 14 days (V4), 90 days (V5) and 180 days (V6). The last evaluation will be performed at V6, after 6 month.
| Arm | Type | Receives |
|---|---|---|
| Glubran® Tiss | Experimental | Procedure: Experimental medical deviceThe application of treatment will be performed by the Investigator that will be instructed for the application of Glutack/Glubran® Tiss 2 system. Glutack® is a user-friendly device for the atraumatic laparoscopic fixation of hernia mesh. Providing precise and consistent delivery of Glubran® Tiss 2/Glubran® 2 with every pull of the trigger, to minimize surgical complications and the potential pain associated with the use of tacks and staples. |
| Glubran® 2 | Active comparator | Procedure: Comparator medical deviceThe application of treatment will be performed by the Investigator that will be instructed for the application of Glutack/Glubran® 2 system. Glutack® is a user-friendly device for the atraumatic laparoscopic fixation of hernia mesh. Providing precise and consistent delivery of Glubran® Tiss 2/Glubran® 2 with every pull of the trigger, to minimize surgical complications and the potential pain associated with the use of tacks and staples. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (14 listed)
- No significant cardiopulmonary, hepatic, or renal impairment, and no contraindications for surgery;
- Clinical diagnosis of:
- Age > 18 years, male and female;
- Obese patient (BMI>35);
- Patients with ASA grade from I to III;
Key exclusion criteria (13 listed)
- Incarcerated hernia;
- Allergy to multiple classes of drugs, recent allergic disease, or use of drugs that are known harmful to vital organs during the 4 weeks before surgery;
- Patients with ASA IV or V;
- Participations in other clinical studies in the 3 months before surgery;
- Atopic allergy history;
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Experimental medical deviceAlso: Glubran TissOpen the blister and pour the sterile single-dose bottle onto the operating table in a sterile field. Before opening the single-dose bottle verify the state of fluidity of the glue and its transparency. Open the single dose of Gluban Tiss® 2. Insert the transfer tip on the single dose, grabbing it near the neck to apply adequate pressure that allows the insertion of the tip. Gradually fill the cartridge by carefully pressing on the body of the single dose. | Procedure or surgery | Glubran® Tiss |
| Comparator medical deviceAlso: Glubran 2Open the blister and pour the sterile single-dose bottle onto the operating table in a sterile field. Before opening the single-dose bottle verify the state of fluidity of the glue and its transparency. Open the single dose of Glubran® 2. Insert the transfer tip on the single dose, grabbing it near the neck to apply adequate pressure that allows the insertion of the tip. Gradually fill the cartridge by carefully pressing on the body of the single dose. | Procedure or surgery | Glubran® 2 |
Primary outcome
Effectiveness
Time frame: Verification of hernia recurrence at 1 day, 1 or 2 weeks, 3 months, 6 months
A clinical examination will be conducted to evaluate recurrence. If there will be any suspicion of recurrence, an ultrasound, MRI or CT is performed according to hospital practice to distinguish true hernia recurrences from bulging. Technical success of glue fastening will be evaluated intra-operatively, the investigator will register whether mesh fixation system achieved technical success or not. Technical success is defined as successful hernia repair as intended.
5 secondary outcomes
Clinical Safety:
Time frame: Verification of Clinical safety at 1 day, 1 or 2 weeks, 3 months, 6 months
Chronic pain
Time frame: Verification of chronic pain at 3 months, 6 months
Quality of the life
Time frame: Verification of QoL at 1 day, 1 or 2 weeks, 3 months, 6 months
Cost effectiveness
Time frame: Verification of cost effectiveness at 1 day, 1 or 2 weeks, 3 months, 6 months
Appropriateness
Time frame: Verification of Appropriateness at Intervention day during the procedure
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 17 Jun 2024.
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Experimental medical device and Comparator medical device in people with Inguinal and Ventral Hernia Repair by Sublay, Underlay and IPOM Mesh Fixation, run by GEM SRL at 1 site in Italy.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 14 inclusion and 13 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 17 Jun 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Effectiveness (time frame: Verification of hernia recurrence at 1 day, 1 or 2 weeks, 3 months, 6 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Jun 2024.