Clinical trials: Abdominal Hernia
Umbilical Hernia Repair, Epigastric Hernia Repair
Outpatient Department Repair of Small Primary Ventral Hernias
Ventral hernias are among the most common conditions requiring surgical intervention. Due to their benign nature, elective repairs of primary ventral hernias are usually given low priority for planned surgery.
- Conditions
- Umbilical Hernia Repair, Epigastric Hernia Repair, Primary Ventral and Incisional Hernia Repair
- Trial name
- OPD-R (NCT07351760)
- Testing
- Outpatient department repair
- Where
- Sweden
- Volunteers
- 37 people
- Sponsor
- Karolinska Institutet
Hernia, Hernia, Ventral
Preoptimisation in Ventral Hernia Surgery
The study is a multicentre, single-blinded, randomised controlled trial. Ventral hernia patients with an aperture width between four and eight centimetres are randomised to either participation in a multimodal preoptimisation…
- Conditions
- Hernia, Hernia, Ventral, Hernia Incisional, Hernia, Umbilical
- Trial name
- PreOpt (NCT07316426)
- Testing
- preoptimisation programme
- Where
- 5 sites in Sweden
- Volunteers
- 130 people
- Sponsor
- Umeå University
Inguinal Hernia
Mesh Fixation inTEP Inguinal Hernia Repair
Mesh fixation is used to prevent recurrence in TEP to the potential cost of pain. The aim was to evaluate the impact of permanent fixation (PF) versus non-permanent fixation (N-PF) of mesh in TEP repair for a primary inguinal…
- Trial name
- register (NCT02419950)
- Testing
- Fixation of mesh in TEP
- Where
- Sweden
- Volunteers
- 1,110 people
- Sponsor
- Skane University Hospital
Obesity, Ventral Hernia
Does a Virtual Coach Offer a Better Solution for Weight Reduction in Ventral Hernia Patients With Obesity?
The purpose for this research is to create a MyChart-enabled virtual coach that assists obese patients lose weight prior to ventral hernia surgery.
- Trial name
- NCT05797974
- Testing
- MyChart enabled virtual weight loss coach, Standard preoperative weight loss tools
- Where
- United States
- Volunteers
- 32 people, healthy volunteers welcome
- Sponsor
- University of Florida
Inguinal Hernia
Swing-Mesh™ Study (SMS).
This multicenter, prospective observational study aims to assess the safety and efficacy of the Swing-Mesh™ implant (THT BioScience™, distributed by B.
- Trial name
- SMS (NCT06915155)
- Testing
- Swing-Mesh™
- Where
- 2 sites in Poland
- Volunteers
- 323 people
- Sponsor
- Swissmed Hospital
Inguinal Hernia
Sutured Versus Cyanoacrylate Glue Mesh Fixation for Inguinal Hernia Repair
Because it avoids direct nerve irritation or entrapment, mesh fixation with tissue adhesive glue seems an optimal option to reduce postoperative pain.
- Trial name
- NCT04203940
- Testing
- Cyanoacryale, Suture
- Where
- Egypt
- Volunteers
- 40 people
- Sponsor
- Mansoura University
Congenital Diaphragmatic Hernia
Fetal Endoscopic Tracheal Occlusion (FETO) Trial for Congenital Diaphragmatic Hernia (CDH)
This is a single site pilot trial to assess the feasibility and safety of treating severe CDH with Fetal Endoscopic Tracheal Occlusion with the Goldballoon Detachable Balloon (GOLDBAL2) along with the Delivery Microcatheter…
- Trial name
- FETO (NCT04052828)
- Testing
- FETO with Goldballoon Detachable Balloon (GOLDBAL2) along with the Delivery Microcatheter (BALTACCI-BDPE100)
- Where
- United States
- Volunteers
- 4 people
- Sponsor
- Dr Erin Perrone
Hernia, Direct Inguinal Hernia
Study on Effects of Defect Closure in Laparoscopic Repair of Direct Inguinal Hernia
The defect closure was found to have higher pain and less seroma formation at various intervals of time following TEP for moderate-large direct inguinal hernia.
- Conditions
- Hernia, Direct Inguinal Hernia, Seroma Following Procedure
- Trial name
- NCT06389331
- Testing
- closed the defect with barbed suture
- Where
- Nepal
- Volunteers
- 88 people
- Sponsor
- B.P. Koirala Institute of Health Sciences
Incisional Hernia, Surgical Site Infection
Prophylactic Mesh Reinforcement for Stoma Closure
In the current work we are aiming to compare between the mesh-reinforced stoma closure and the anatomical closure in terms of the risk of developing surgical site incisional hernia (SSIH),incidence of surgical site infection …
- Conditions
- Incisional Hernia, Surgical Site Infection, Postoperative Pain, Hospital Stay, Length of Stay in Hospital From Surgery to Discharge
- Trial name
- OASIS (NCT06157645)
- Testing
- Prolene mesh
- Where
- Egypt
- Volunteers
- 62 people
- Sponsor
- Assiut University
Congenital Diaphragmatic Hernia
Initiation of Resuscitation While Attached to the Cord With Congenital Diaphragmatic Hernia
This study aims to measure the cardio-respiratory physiological consequences of initiating resuscitation during placental transfusion (PT) with an intact umbilical cord in infants with congenital diaphragmatic hernia (CDH).
- Trial name
- INSPIRE-CDH (NCT03094039)
- Testing
- Ventilatory support while attached to the cord, Immediate cord clamping
- Where
- Canada
- Sponsor
- University of Alberta
Hernia, Ventral, Rectus Diastasis
Endoscopic eTEP Versus Open Rives-Stoppa
Observational cohort study (partially retrospective, partially prospective) comparing the endoscopic extended totally extraperitoneal prosthesis (eTEP) repair for midline abdominal hernias to open Rives-Stoppa repair (control).
- Trial name
- NCT05446675
- Testing
- Endoscopic eTEP, Open Rives-Stoppa
- Where
- Belgium
- Volunteers
- 60 people
- Sponsor
- AZ Alma
Inguinal Hernia Repair, Inguinal Hernia
Non-mesh Repair of Inguinal Hernia: Desarda Versus Darn
To compare the results of Desarda and Darn techniques in inguinal hernia repair in Assiut University Hospital.
- Trial name
- NCT06712212
- Testing
- Inguinal Hernias repair: Desarda, Inguinal hernia repair: Darn
- Where
- Egypt
- Volunteers
- 30 people
- Sponsor
- Assiut University
Bariatric Surgery Candidate, Hiatal Hernia
Safety and Feasibility of Liver Retraction With the Levita Magnetic Surgical System: Extended Magnetic Grasper Device
The purpose of this study is to evaluate the safety and effectiveness of the Extended Magnetic Grasper Device in patients undergoing bariatric and/or hiatal hernia procedures, as a liver retractor grasping the liver and/or the…
- Trial name
- NCT06432088
- Testing
- Extended Magnetic Grasper Device
- Where
- Chile
- Volunteers
- 30 people
- Sponsor
- Levita Magnetics
Congenital Diaphragmatic Hernia
Engagement in Physical Activities and Sports in Adolescents With Diaphragmatic Hernia
The objective is to understand how a population of adolescents - who have undergone diaphragm surgery within their first month of life (i.e.
- Trial name
- CHASAM (NCT05666986)
- Where
- France
- Volunteers
- 20 people, healthy volunteers welcome
- Sponsor
- University Hospital, Lille
Inguinal Hernia, Chronic Pain
Chronic Pain After Inguinal Hernia Repair
Chronic pain after inguinal hernia repair has become a major concern. Although tension-free Lichtenstein technique is used and new lightweight meshes have been developed, still up to 40 % of patients complain of some kind of pain…
- Trial name
- GRIP-ME (NCT00820131)
- Testing
- selfgrip mesh, lightweight mesh with suture fixation
- Where
- 7 sites in Austria
- Volunteers
- 250 people
- Sponsor
- Medical University of Vienna
Congenital Diaphragmatic Hernia
Fetal Endoscopic Tracheal Occlusion (FETO) for Severe Congenital Diaphragmatic Hernia
The purpose of the study is to study the efficacy of fetal endoscopic tracheal occlusion (FETO) in cases of severe congenital diaphragmatic hernia (CDH).
- Trial name
- FETO (NCT05461222)
- Testing
- Balt "Goldballoon"
- Where
- United States
- Volunteers
- 15 people
- Sponsor
- Yair Blumenfeld
Inguinal Hernia
Effect of Suture for Mesh Fixation in Lichtenstein Hernia Repair
The investigators want to evaluate the effect of suturing the mesh versus using a self-adhesive mesh for Lichtenstein hernia repair. Effect parameters include chronic pain.
- Trial name
- Dangrip (NCT00815698)
- Testing
- suture, no suture
- Where
- 5 sites in Denmark
- Volunteers
- 334 people
- Sponsor
- Jacob Rosenberg
Inguinal Hernia
Activity Restrictions After Inguinal Hernia Repair
This research is intended to be a pilot study to identify differences in outcomes for varied lifting and physical activity precautions following surgical repair of single-sided inguinal hernias.
- Trial name
- NCT05867134
- Testing
- Removal of postoperative lifting restrictions
- Where
- United States
- Volunteers
- 200 people, healthy volunteers welcome
- Sponsor
- VA Eastern Colorado Health Care System
Hernia
Safety Study of MotifMESH (cPTFE) in Abdominal Surgery
This study will monitor surgically repaired large abdominal hernias requiring condensed fenestrated polytetrafluoroethylene mesh (cPTFE).
- Trial name
- NCT01364233
- Testing
- MotifMESH
- Where
- United States
- Volunteers
- 10 people
- Sponsor
- Medline Industries
Incisional Hernia Occurence
Assessment of Risk Factors for Incisional Hernia Following Major Abdominal Surgery
The aim of this study is to assess the independent patient-related and surgery-related risk factors associated with the development of incisional hernia following major abdominal surgeries.
- Trial name
- NCT07790172
- Testing
- cases, controls
- Where
- Egypt
- Volunteers
- 100 people
- Sponsor
- Sohag University
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