Pilonidal DiseaseNCT03458663
Randomized Trial Comparing Prevena and ActiV.A.C. System to Convetional Care After Bascom's Cleft Lift Surgery
A study testing Prevena™ og ACTIV.A.C™ Therapy System. in people with Pilonidal Disease, run by University of Aarhus at 1 site in Denmark.
Trial summary
In a single-blinded randomized, controlled study design the investigators wish to examine to effect of Prevena + ActiV.A.C. therapy system on the postoperative healing in patients operated for chronic pilonidal disease using Bascoms' Cleft Lift procedure. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Pilonidal Disease
- What is being tested?
- Prevena™ og ACTIV.A.C™ Therapy System.
- Type of treatment
- Pill or oral medicine, Medical device
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 106 participants
- Where
- 1 siteDenmark
- Study dates
- 14 Jan 2019to 1 Apr 2022
- 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
- Patients with recurrence after previous surgery for pilonidal disease, cases of poor postoperative healing (> two months) or primary extensive/fistulating disease referred to Randers Regional Hospital for assessment for reconstructive BCL surgery.
Who cannot join
- Patients under 18 years of age
- Patients who smoke (not offered this type of surgery), ceased min. 6 weeks pre-operatively
- Patients with PS lesions are ≤ 3 cm from the anus
- Patients with allergies to Silver or acrylic
- Patients who cannot adhere to study protocol
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Single-blinded, Randomized Study Comparing Healing After Bascom's Cleft Lift Operation for Pilonidal Disease With or Without Prevena ™ and ACTIV.A.C ™ Therapy System
In a single-blinded randomized, controlled study design the investigators wish to examine to effect of Prevena + ActiV.A.C. therapy system on the postoperative healing in patients operated for chronic pilonidal disease using Bascoms' Cleft Lift procedure. At the department of surgery at The regional Hospital i Randers Denmark the investigators handle cases from the entire region and have a decent patient volume. The investigators have used Bascoms' Cleft left since 2013 and registered complications and experience wound deshisseance or prolonged healing in approx. 15% causing the investigators to challange the postoperative regime.
Read the detailed description
Background Pilonidal disease (PS) is a common disorder that occurs in the crena ani. A paradigm shift of our perception of the pathology of this disorder has been on its way for several decades and the treatment is slowly starting to follow.
The estimated incidence is 26 per 100,000 although this is subject to large geographical variation. Men present themselves with symptomatic pilonidal disease more than twice as often as women and in population surveys of young students, a 10: 1 male / female ratio has been found, including also asymptomatic pilonidal cysts. The disorder usually affects the younger population with average age at first manifestation of 21 years for men and 19 for women.
Acute manifestations are infected and result in pilonidal abscesses. The treatment of acute abscesses within pilonidal disease is uncontroversial and is based on lateral incision and drainage with subsequent open healing.
The treatment of chronic pilonidal disease, on the other hand, is still controversial. Traditional surgical approach is based on excision of the affected tissue with primary closure or open secondary healing. This treatment, regardless of the manifestation of disease, is characterized by poor healing, complicated postoperative ulceration and recurrence.
Since April 2010, there has been a combination and standardization of the treatment of complicated pilonidal disease at the regional hospital in Randers (Denmark), where patients with 1) recurrence after previous surgery, 2) missing healing > 2 months after surgery and 3) extensive / fistulatory pilonidal disease are offered Bascom's cleft lift (BCL ) operation for the condition.
Bascoms Cleft Lift operation is one of several lateralization techniques that have shown promising results over the last decades. It has the significant advantage compared to the other generally accepted surgical lateralization techniques that it only removed a skin patch (7 mm thick); sub cutis and fat is left in situ regardless of its involvement in the condition: Crena anii is lifted and lateralized, thereby solving the underlying problem and preserving most tissues. The intervention should be significantly less painful than other variants.
In the ongoing work it has been clear that there is delayed healing in a large proportion of these patients by the scheduled postoperative control 14 days after surgery. During the experience of the investigators throughout the first 3 years wound healing complications / delayed healing was found to a variable extent. More than 15% were followed longer than 3 months due to delayed healing and nearly 7% had to be re-operated due to primarily undermining of the cicatrices.
As the operating results are otherwise promising in these recurrent patients, the investigators find it relevant to optimize the postoperative course focusing on better healing.
A vacuum assisted (negative pressure) system, Prevena ™ and ACTIV.A.C ™ therapy system has been developed to maintain drainage on closed incisions. The system also works by altering the cytokine profile locally so that it functions anti-inflammatory, by increasing local growth factors and promoting angiogenesis19. Negative pressure wound management (NPWM) such as Prevena ™ and ACTIV.AC ™ is a widely used tool with many different variations, but the evidence of effect remains sparse and more studies are required. The investigators believe that in a dry and closed incision such as the one after BCL surgery, in an area exposed to stretching during healing, it must be an advantage of maintaining drainage, reducing the anti-inflammatory response and increasing angiogenesis.
Hypothesis
The investigators hypothesize that:
- Patients who have undergone BCL surgery for complicated pilonidal disease have a significantly better healing using Prevena ™ and ACTIV.A.C ™ Therapy System 4-7 days post-operatively compared to patients undergoing normal regimen with drainage and conventional wound dressing.
- That the optimized healing will positively affect the health and wellbeing of patients.
The investigators are not aware of other studies that examine the effect of healing with or without Prevena ™ and ACTIV.A.C ™ or similar devices or its effects on the quality of life of these patients.
Purpose of the study
- To investigate whether Prevena ™ and ACTIV.A.C ™ Therapy System after BCL surgery for complicated pilonidal disease will improve wound healing compared to a control group of patients treated with conventional drainage and dressing.
- To examine whether Prevena ™ and ACTIV.A.C ™ treatment and possibly faster healing after surgery for PS affects the self-perceived and pain after surgery using questionnaires / pain journal (Appendix 2 and 3).
- To describe general health perception among patients with complicated pilonidal disease before and after Bascom's Cleft Lift operation using a questionnaire regarding pilonidal disease.
- To investigate whether postoperative pain after BCL surgery for complicated pilonidal decreases with Prevena ™ and ACTIV.A.C ™ Therapy System.
Primary end point:
- Evaluate the clinical effect* of Prevena ™ and ACTIV.AC ™ of 4-7 days on BCL cicatrices after 14 days of healing by the following two criteria*: 1) existence of defects in the cicatricees (defects ≤ 5 mm considered fully healed) and 2) undermining of the cicatrices.
Secondary end point:
Evaluate the following short and long term results in connection with BCL surgery and the use of Prevena ™ and ACTIV.A.C ™ Therapy System:
- Symptom related health perception assessed baseline, 14 days postoperatively, after 3 months and after 12 months assessed by questionnaire (Appendix 2)
- Healing after 3 months evaluated according to criteria described above
- Recurrence rate
- Postoperative pain assessed by pain diary (Appendix 3)
- Conditions
- Pilonidal Disease
- Being tested
- Prevena™ og ACTIV.A.C™ Therapy System.
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Prevena™ og ACTIV.A.C™ Therapy System.Device
A vacuum assisted (negative pressure) system, Prevena ™ and ACTIV.A.C ™ therapy system have been developed to maintain drainage on closed incisions. The system also works by altering the cytokine profile locally so that it functions anti-inflammatory, by increasing local growth factors and promoting angiogenesis19. Negative pressure wound management (NPWM) such as Prevena ™ and ACTIV.AC ™ is a widely used tool with many different variations, but the evidence of effect remains sparse and more studies are required20. We believe that in a dry and closed incision such as the one after BCL surgery, in an area exposed to stretching during healing, it must be an advantage of maintaining drainage, reducing the anti-inflammatory response and increasing angiogenesis.
| Study group | Role | What they receive |
|---|---|---|
| Prevena | Experimental | Patients randomized to application of Prevena ™ and ACTIV.A.C ™ Therapy System 4-7 days post-operatively. Patients will return to the surgical day clinic to have the system removed either at day 7 or when/ if function ceases. Patients receive 3 days oral antibiotics postoperatively (Ciproxin 250 mg x 2 and Metronidazole 500 mg x 3). Sutures are removed at clinical control after 14 days and patients are seen again by BCL surgeon after 3 months and are discharged when completely healeddrainage and conventional wound dressing Receives: Device: Prevena™ og ACTIV.A.C™ Therapy System. |
| Conentional postoperative care | No intervention | patients randomized to convetional postoperative regime with a penrose drain (passive) and a dry draping for 24 hours and after usage of sanitary pads. Patients receive 3 days oral antibiotics postoperatively (Ciproxin 250 mg x 2 and Metronidazole 500 mg x 3). Drain is removed after 24 hours and Sutures are removed at clinical control after 14 days and patients are seen again by BCL surgeon after 3 months and are discharged when completely healeddrainage and conventional wound dressing. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Primary healing
Evaluation of BCL cicatrices after 14 days of healing by the following two criteria*: 1) existence of defects in the cicatricees (defects ≤ 5 mm considered fully healed) and 2) undermining of the cicatrices.
Measured: 14 days after surgery
Secondary outcomes (4)
Health perception
Symptom related health perception assessed baseline, 14 days postoperatively, after 3 months and after 12 months assessed by questionnaire
Measured: upto 12 months after surgery
Long term healing
Healing after 3 months evaluated according to criteria described previously
Measured: 3 months after surgery
early recurrence
record recurrence
Measured: up to 12 months after surgery
post operative pain
Postoperative pain assessed by pain diary
Measured: 14 days after surgey
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted8 Mar 2018
- Study start14 Jan 2019
- Primary completion1 Mar 2022
- Study completion1 Apr 2022
Why it stopped: Interrim analysis showed no effect or a tendency towards poorer out come in the Prevena group
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Pilonidal DiseaseStudies 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
- Supportive care
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Single blinded, randomized controlled trial .
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 106 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Aarhus
- Sponsor type
- University, hospital or other
- Collaborators
- Randers Regional Hospital
- Responsible party
- Sponsor
- Investigators
- susanne Haas, Principal investigator, Clinical officer
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03458663
- Sponsor's protocol ID
- RCTBCL2018
- Status last verified
- May 2022
- First submitted
- 2 Mar 2018
- Last updated
- 19 May 2022
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: There is not. Data will be handled and analysed within our unit
Study at a glance
From the registry record, last updated by the sponsor on 19 May 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Single-blinded, Randomized Study Comparing Healing After Bascom's Cleft Lift Operation for Pilonidal Disease With or Without Prevena ™ and ACTIV.A.C ™ Therapy System
- ClinicalTrials.gov ID
- NCT03458663
- Acronym / sponsor ID
- RCTBCL2018
- Conditions
- Pilonidal Disease
- Study type
- Interventional
- Recruitment status
- TerminatedReason stopped: Interrim analysis showed no effect or a tendency towards poorer out come in the Prevena group
- Enrolment
- 106 participants (actual)
- Lead sponsor
- University of AarhusUniversity, hospital or other
- Collaborators
- Randers Regional Hospital
- Study start
- 14 Jan 2019 (actual)
- Primary completion
- 1 Mar 2022 (actual)
- Study completion
- 1 Apr 2022 (actual)
- First posted
- 8 Mar 2018 (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.
In a single-blinded randomized, controlled study design the investigators wish to examine to effect of Prevena + ActiV.A.C. therapy system on the postoperative healing in patients operated for chronic pilonidal disease using Bascoms' Cleft Lift procedure. At the department of surgery at The regional Hospital i Randers Denmark the investigators handle cases from the entire region and have a decent patient volume. The investigators have used Bascoms' Cleft left since 2013 and registered complications and experience wound deshisseance or prolonged healing in approx. 15% causing the investigators to challange the postoperative regime.
Detailed description
Background Pilonidal disease (PS) is a common disorder that occurs in the crena ani. A paradigm shift of our perception of the pathology of this disorder has been on its way for several decades and the treatment is slowly starting to follow.
The estimated incidence is 26 per 100,000 although this is subject to large geographical variation. Men present themselves with symptomatic pilonidal disease more than twice as often as women and in population surveys of young students, a 10: 1 male / female ratio has been found, including also asymptomatic pilonidal cysts. The disorder usually affects the younger population with average age at first manifestation of 21 years for men and 19 for women.
Acute manifestations are infected and result in pilonidal abscesses. The treatment of acute abscesses within pilonidal disease is uncontroversial and is based on lateral incision and drainage with subsequent open healing.
The treatment of chronic pilonidal disease, on the other hand, is still controversial. Traditional surgical approach is based on excision of the affected tissue with primary closure or open secondary healing. This treatment, regardless of the manifestation of disease, is characterized by poor healing, complicated postoperative ulceration and recurrence.
Since April 2010, there has been a combination and standardization of the treatment of complicated pilonidal disease at the regional hospital in Randers (Denmark), where patients with 1) recurrence after previous surgery, 2) missing healing > 2 months after surgery and 3) extensive / fistulatory pilonidal disease are offered Bascom's cleft lift (BCL ) operation for the condition.
Bascoms Cleft Lift operation is one of several lateralization techniques that have shown promising results over the last decades. It has the significant advantage compared to the other generally accepted surgical lateralization techniques that it only removed a skin patch (7 mm thick); sub cutis and fat is left in situ regardless of its involvement in the condition: Crena anii is lifted and lateralized, thereby solving the underlying problem and preserving most tissues. The intervention should be significantly less painful than other variants.
In the ongoing work it has been clear that there is delayed healing in a large proportion of these patients by the scheduled postoperative control 14 days after surgery. During the experience of the investigators throughout the first 3 years wound healing complications / delayed healing was found to a variable extent. More than 15% were followed longer than 3 months due to delayed healing and nearly 7% had to be re-operated due to primarily undermining of the cicatrices.
As the operating results are otherwise promising in these recurrent patients, the investigators find it relevant to optimize the postoperative course focusing on better healing.
A vacuum assisted (negative pressure) system, Prevena ™ and ACTIV.A.C ™ therapy system has been developed to maintain drainage on closed incisions. The system also works by altering the cytokine profile locally so that it functions anti-inflammatory, by increasing local growth factors and promoting angiogenesis19. Negative pressure wound management (NPWM) such as Prevena ™ and ACTIV.AC ™ is a widely used tool with many different variations, but the evidence of effect remains sparse and more studies are required. The investigators believe that in a dry and closed incision such as the one after BCL surgery, in an area exposed to stretching during healing, it must be an advantage of maintaining drainage, reducing the anti-inflammatory response and increasing angiogenesis.
Hypothesis
The investigators hypothesize that:
- Patients who have undergone BCL surgery for complicated pilonidal disease have a significantly better healing using Prevena ™ and ACTIV.A.C ™ Therapy System 4-7 days post-operatively compared to patients undergoing normal regimen with drainage and conventional wound dressing.
- That the optimized healing will positively affect the health and wellbeing of patients.
The investigators are not aware of other studies that examine the effect of healing with or without Prevena ™ and ACTIV.A.C ™ or similar devices or its effects on the quality of life of these patients.
Purpose of the study
- To investigate whether Prevena ™ and ACTIV.A.C ™ Therapy System after BCL surgery for complicated pilonidal disease will improve wound healing compared to a control group of patients treated with conventional drainage and dressing.
- To examine whether Prevena ™ and ACTIV.A.C ™ treatment and possibly faster healing after surgery for PS affects the self-perceived and pain after surgery using questionnaires / pain journal (Appendix 2 and 3).
- To describe general health perception among patients with complicated pilonidal disease before and after Bascom's Cleft Lift operation using a questionnaire regarding pilonidal disease.
- To investigate whether postoperative pain after BCL surgery for complicated pilonidal decreases with Prevena ™ and ACTIV.A.C ™ Therapy System.
Primary end point:
- Evaluate the clinical effect* of Prevena ™ and ACTIV.AC ™ of 4-7 days on BCL cicatrices after 14 days of healing by the following two criteria*: 1) existence of defects in the cicatricees (defects ≤ 5 mm considered fully healed) and 2) undermining of the cicatrices.
Secondary end point:
Evaluate the following short and long term results in connection with BCL surgery and the use of Prevena ™ and ACTIV.A.C ™ Therapy System:
- Symptom related health perception assessed baseline, 14 days postoperatively, after 3 months and after 12 months assessed by questionnaire (Appendix 2)
- Healing after 3 months evaluated according to criteria described above
- Recurrence rate
- Postoperative pain assessed by pain diary (Appendix 3)
Study design
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 2
- Model description
- Single blinded, randomized controlled trial .
| Arm | Type | Receives |
|---|---|---|
| Prevena | Experimental | Device: Prevena™ og ACTIV.A.C™ Therapy System.Patients randomized to application of Prevena ™ and ACTIV.A.C ™ Therapy System 4-7 days post-operatively. Patients will return to the surgical day clinic to have the system removed either at day 7 or when/ if function ceases. Patients receive 3 days oral antibiotics postoperatively (Ciproxin 250 mg x 2 and Metronidazole 500 mg x 3). Sutures are removed at clinical control after 14 days and patients are seen again by BCL surgeon after 3 months and are discharged when completely healeddrainage and conventional wound dressing |
| Conentional postoperative care | No intervention | –patients randomized to convetional postoperative regime with a penrose drain (passive) and a dry draping for 24 hours and after usage of sanitary pads. Patients receive 3 days oral antibiotics postoperatively (Ciproxin 250 mg x 2 and Metronidazole 500 mg x 3). Drain is removed after 24 hours and Sutures are removed at clinical control after 14 days and patients are seen again by BCL surgeon after 3 months and are discharged when completely healeddrainage and conventional wound dressing. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (1 listed)
- Patients with recurrence after previous surgery for pilonidal disease, cases of poor postoperative healing (> two months) or primary extensive/fistulating disease referred to Randers Regional Hospital for assessment for reconstructive BCL surgery.
Key exclusion criteria (5 listed)
- Patients under 18 years of age
- Patients who smoke (not offered this type of surgery), ceased min. 6 weeks pre-operatively
- Patients with PS lesions are ≤ 3 cm from the anus
- Patients with allergies to Silver or acrylic
- Patients who cannot adhere to study protocol
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 |
|---|---|---|
| Prevena™ og ACTIV.A.C™ Therapy System.A vacuum assisted (negative pressure) system, Prevena ™ and ACTIV.A.C ™ therapy system have been developed to maintain drainage on closed incisions. The system also works by altering the cytokine profile locally so that it functions anti-inflammatory, by increasing local growth factors and promoting angiogenesis19. Negative pressure wound management (NPWM) such as Prevena ™ and ACTIV.AC ™ is a widely used tool with many different variations, but the evidence of effect remains sparse and more studies are required20. We believe that in a dry and closed incision such as the one after BCL surgery, in an area exposed to stretching during healing, it must be an advantage of maintaining drainage, reducing the anti-inflammatory response and increasing angiogenesis. | Device | Prevena |
Primary outcome
Primary healing
Time frame: 14 days after surgery
Evaluation of BCL cicatrices after 14 days of healing by the following two criteria*: 1) existence of defects in the cicatricees (defects ≤ 5 mm considered fully healed) and 2) undermining of the cicatrices.
4 secondary outcomes
Health perception
Time frame: upto 12 months after surgery
Long term healing
Time frame: 3 months after surgery
early recurrence
Time frame: up to 12 months after surgery
post operative pain
Time frame: 14 days after surgey
Results and safety
The study was stopped early (reason given: Interrim analysis showed no effect or a tendency towards poorer out come in the Prevena group). Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 19 May 2022.
- Individual participant dataSharing planned: No. There is not. Data will be handled and analysed within our unit
Related trials for Pilonidal Disease
Recruiting
Pilot Trial Assessing the Effectiveness of Laser Hair Depilation on Pilonidal Disease Recurrence in Patients With Darker Skin Color
Pilonidal Disease
Recruiting
VAAPS Combined With Loose Seton Drainage for Postoperative Self-Care: A Prospective Single-Arm Cohort Study
Pilonidal Sinus Disease
Not yet recruiting
Teach-Back Discharge Education After Pilonidal Sinus Surgery
Pilonidal Sinus Disease, Pilonidal Sinus Treatment
Recruiting
LASER VERSUS CRYSTALLIZED PHENOL IN PILONIDAL SINUS DISEASE
Sacrococcygeal Pilonidal Sinus Disease, Pilonidal Sinus Disease
Recruiting
Intraoperative Wound Irrigation for Pilonidal Disease
Pilonidal Disease
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.
susanne Haas principal investigator
Clinical officer
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Prevena™ og ACTIV.A.C™ Therapy System. in people with Pilonidal Disease, run by University of Aarhus at 1 site in Denmark.
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 1 inclusion and 5 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: stopped early, as of the sponsor's last update on 19 May 2022. 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 Denmark. 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 was stopped early (reason given: Interrim analysis showed no effect or a tendency towards poorer out come in the Prevena group). Results are not available in the source record.
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?
Primary healing (time frame: 14 days after surgery). 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 19 May 2022; AzTrials last refreshed its copy on 29 Oct 2026.