Clinical trials: Ventral Hernias
Umbilical Hernia
Cosmetic Outcomes of Umbilical Hernia Incisions
This will be a single institution, prospective, randomized controlled trial. Patients presenting as an outpatient for repair of umbilical hernias who meet our inclusion criteria, whose parents provide permission to participate in…
- Trial name
- UHR (NCT06738121)
- Testing
- Infra-umbilical incision, Transumbilical incision
- Where
- United States
- Volunteers
- 2 people
- Sponsor
- Children's Mercy Hospital Kansas City
Sensation of Inadequate Defecation, Rectal Prolapse
Surgical Treatment of Obstructed Defecation Syndrome
Obstructed Defecation is a profoundly disabling condition. Many different surgical procedures has been introduced to treat patients affected by this disease. The most used are STARR and ventral rectopexy.
- Conditions
- Sensation of Inadequate Defecation, Rectal Prolapse, Rectocele
- Trial name
- PRO-REST (NCT01899209)
- Testing
- STARR, Laparoscopic Ventral Rectopexy
- Where
- Italy
- Volunteers
- 40 people
- Sponsor
- IRCCS Azienda Ospedaliero-Universitaria di Bologna
Hernia, Ventral
Cost- Effectiveness and Cost-utility of Laparoscopic Versus Open Repair of Ventral Hernia
The purpose of this prospective paper is to make a comparison between laparoscopic and opening approaches in ventral hernia repair, taking into account absence of recurrence in long - time (5 years), results centered at patient…
- Trial name
- NCT01778387
- Testing
- Laparoscopic ventral hernia repair
- Where
- Spain
- Volunteers
- 130 people
- Sponsor
- Fundación Andaluza Beturia para la Investigación en Salud
Ventral Hernia
Negative Pressure Incisional Wound Therapy for High-risk Ventral Hernia Repair
The investigators are testing the ability of vacuum dressings to improve wound healing for patients having large hernias surgically repaired who are at risk of having wound complications.
- Trial name
- N-PITH (NCT04455724)
- Testing
- Negative pressure incisional wound therapy, Standard sterile dressing
- Where
- Canada
- Volunteers
- 110 people, healthy volunteers welcome
- Sponsor
- McMaster University
Ventral Hernia
Bariatric SUrgery With Mesh REpair of Ventral Hernia: a Randomized Controlled Trial
The primary objective of the study is to demonstrate that hernia recurrence (VH) repair with non absorbable mesh concomitant to Bariatric Surgery (BS) decreases the risk of VH, with or without surgical repair, during the first…
- Trial name
- BeSURE (NCT05488288)
- Testing
- Mesh repair, Suture repair
- Where
- France
- Volunteers
- 354 people
- Sponsor
- Assistance Publique - Hôpitaux de Paris
Ventral Hernia
Sutured vs Sutureless Mesh Fixation for Onlay Ventral Hernia Repair
Comparison beta sutured and suturless mesh fixation for ventral hernia regarding recurrence rates and complications rate
- Trial name
- NCT06209450
- Testing
- Ventral hernia repair with mesh fixation
- Volunteers
- 1 people, healthy volunteers welcome
- Sponsor
- Assiut University
Ventral Hernia
Comparative Study of Biologic Mesh Versus Repair With Component Separation.
The purpose of this study is to compare open abdominal incisional hernia repair using XenMATRIX biologic mesh versus repair with their own tissue.
- Trial name
- Davol (NCT01295125)
- Testing
- XenMATRIX mesh, Open abdominal ventral hernia repair
- Where
- United States
- Volunteers
- 9 people, healthy volunteers welcome
- Sponsor
- University Hospitals Cleveland Medical Center
Umbilical Hernia Repair
Topical Tranexamic Acid Spray Versus No Spray on Postoperative Outcomes Following Mesh Repair of Umbilical Hernia
Umbilical hernia is a type of ventral hernia that occurs commonly in adulthood, and mesh reinforcement is well established since there is a reduced recurrence rate when compared to suture repair.
- Trial name
- NCT07845370
- Testing
- Topical Tranexamic Acid Spray, No Topical Tranexamic acid
- Where
- Pakistan
- Volunteers
- 252 people
- Sponsor
- Dr Mudassar Saeed Pansota
Hernia
A Retrospective Study With Prospective Follow-Up of Laparoscopic Ventral Hernia Repair Utilizing the Bard Sepramesh IP Composite
This study will enroll subjects who underwent a laparoscopic ventral hernia repair utilizing Sepramesh at least 12 months before starting in this study.
- Trial name
- Sepramesh (NCT01305473)
- Where
- United States
- Volunteers
- 90 people
- Sponsor
- C. R. Bard
Abdominal Wall Defect
Study to Evaluate Reduction in Pain After Laparoscopic Hernia Repair With Mesh Soaked in Bupivacaine Solution
Early post-operative pain and discomfort after laparoscopic repair remains a concern for patients requiring hospital stay and parenteral narcotic analgesics .
- Trial name
- HAPPIEST (NCT03035617)
- Testing
- Bupivacaine, Saline
- Where
- Pakistan
- Volunteers
- 100 people
- Sponsor
- Aga Khan University