Clinical trials: Hernia, Incisional
Hernia, Ventral, Incisional Hernia
A Prospective Trial of a Bio-absorbable Mesh in Challenging Laparoscopic Ventral or Incisional Hernia Repair
The objective of this study is to collect additional data on safety, performance and effectiveness of Phasix™ ST in subjects receiving laparoscopic ventral or incisional hernia repair at high risk for surgical site occurrence…
- Trial name
- ATLAS (NCT02712398)
- Testing
- Phasix™ ST
- Where
- 16 sites in United States
- Volunteers
- 120 people
- Sponsor
- C. R. Bard
Incisional Hernia
Prevention of Incisional Hernia With Biosynthetic Mesh at the Site of Temporary Ileostomy Closure (PRINCESS)
Prophylactic mesh reinforcement of the abdominal wall at the site of temporary ileostomy closure is effective in preventing postoperative incisional hernia.
- Trial name
- PRINCESS (NCT05400083)
- Where
- Italy
- Volunteers
- 203 people
- Sponsor
- Federico II University
Hernia
BP as a Super-light Mesh and as a New Fixation Device for General Surgery -DM108/2008-B
The Buckypaper (BP) is an innovative material that has attracted the attention of many research groups engaged in the study of its possible applications in various technological fields.
- Trial name
- DM108/2008-B (NCT02341222)
- Testing
- BP self-standing felt device, PR Parietene mesh device
- Where
- Italy
- Volunteers
- 30 people
- Sponsor
- University of Roma La Sapienza
Surgical Incision, Wound Dehiscence
Treating Emergency Laparotomy Incisions With Negative Pressure Wound Therapy
The goal of this clinical trial is to investigate Negative Pressure Wound Therapy (NPWT) in adults undergoing emergency laparotomy.
- Conditions
- Surgical Incision, Wound Dehiscence, Surgical Site Infection, Incisional Hernia
- Trial name
- TELIN (NCT07003906)
- Testing
- Negative pressure wound therapy, Standard postoperative dressing
- Where
- 6 sites in Sweden
- Volunteers
- 720 people
- Sponsor
- Uppsala University
Hernia, Inguinal
SIL-TEP vs TEP for Inguinal Hernia Repair in Day Surgery
This study aim to compare the efficacy and safety of Single incisional Laparoscopic Total Extraperitoneal(SIL-TEP) Inguinal Hernia Repair and traditional Laparoscopic Total Extraperitoneal(TEP) Inguinal Hernia Repair in day…
- Trial name
- NCT02415543
- Testing
- SIL-TEP Inguinal Hernia Repair, TEP Inguinal Hernia Repair
- Where
- China
- Volunteers
- 100 people, healthy volunteers welcome
- Sponsor
- TAO CHEN
Incisional Hernia
Hernia-Prophylaxis in Acute Care Surgery H-PACS
Incisional hernia is a common complication in visceral surgery and varies between 11 and 26% in the general surgical population.
- Trial name
- H-PACS (NCT03090022)
- Testing
- Strattice, Single running suture of abdominal fascia
- Where
- Switzerland
- Volunteers
- 61 people
- Sponsor
- Insel Gruppe AG, University Hospital Bern
Obese Adults, Hernia Abdominal Wall
Tirzepatide-Based Prehabilitation Before Elective Ventral and Incisional Hernia Repair in Patients With Obesity
This study evaluated whether a 16-week weight-loss program using tirzepatide before elective ventral and incisional hernia surgery could improve surgical readiness and outcomes in patients with obesity.
- Conditions
- Obese Adults, Hernia Abdominal Wall, Prehabilitation
- Trial name
- NCT07638592
- Testing
- Tirzepatide prehabilitation
- Where
- Italy
- Volunteers
- 91 people
- Sponsor
- Azienda Sanitaria Locale Napoli 2 Nord
Incisional Hernia
Prevention of Incisional Hernia With an Onlay Mesh Visible on MRI
It has been demonstrated that incisional hernia incidence after laparotomy can be safely reduced with the addition of a mesh to the conventional closure of the abdominal wall.
- Trial name
- VISIBLE (NCT03105895)
- Testing
- Mesh group
- Where
- 5 sites in Spain
- Volunteers
- 200 people
- Sponsor
- Henares University Hospital
Ventral Hernia, Umbilical Hernia
Does a Transabdominal Plane Block Decrease Patient Pain After Ventral Hernia Repair?
The purpose of this study is to determine if a Transabdominal Plane Block will decrease patient pain and pain medication use after a laparoscopic ventral (ventral, umbilical, incisional) hernia repair with mesh.
- Conditions
- Ventral Hernia, Umbilical Hernia, Incisional Hernia, Postoperative Complications
- Trial name
- NCT02007096
- Testing
- Transabdominal Plane Block, Non Transabdominal Plane Block
- Where
- United States
- Volunteers
- 127 people, healthy volunteers welcome
- Sponsor
- Icahn School of Medicine at Mount Sinai
Incisional Hernia, Emergency Laparotomy
Preemer Trial - Prophylactic Mesh Versus no Mesh in the Midline Emergency Laparotomy Closure for Prevention of Incisional Hernia: a Multi Center, Double-blind, Randomized Controlled Trial
244 patients, who have an emergency midline laparotomy for any gastrointestinal reason, will be randomized in a 1:1 ratio either to mesh group with a retrorectus prophylactic self-gripping mesh or to control group with 4:1 small…
- Conditions
- Incisional Hernia, Emergency Laparotomy, Midline Laparotomy, Hernia Prevention
- Trial name
- NCT04311788
- Testing
- Prophylactic self gripping mesh, Slowly absorbable continuous monofilament suture
- Where
- 7 sites in Finland
- Volunteers
- 109 people
- Sponsor
- University of Oulu
Ventral Incisional Hernia
Tension in Posterior Component Separation for Abdominal Wall Reconstruction
The purpose of this study is to measure the changes in tension after each release in a standard posterior component separation during abdominal wall reconstruction.
- Trial name
- NCT05142761
- Where
- United States
- Volunteers
- 100 people, healthy volunteers welcome
- Sponsor
- Michael Rosen
Wound Infection, Incisional Hernia
When Closing Midline Incisions, do Small Stitches Reduce the Risk for Incisional Hernia, Wound Infection or Dehiscence?
The purpose of this study is to determine whether a technique using very small stitches when closing a midline incision can reduce the risk for wound complications such as incisional hernia, infection or dehiscence.
- Conditions
- Wound Infection, Incisional Hernia, Wound Dehiscence
- Trial name
- NCT00508053
- Testing
- Small stitches, Mass closure
- Where
- Sweden
- Volunteers
- 737 people
- Sponsor
- Sundsvall Hospital
Incisional Hernia, Wound Dehiscence
Hernia After Colorectal Cancer Surgery
Defects in the abdominal wall (incisional hernia) is a frequent negative outcome after surgery. Reinforcing the incision with mesh seem to lower the incidence but in surgery that includes bowel resection a simple alternative…
- Conditions
- Incisional Hernia, Wound Dehiscence, Wound Complication, Quality of Life
- Trial name
- Rein4CeTo1 (NCT03390764)
- Testing
- 4:1 closure group, RTL plus 4:1 closure group
- Where
- Sweden
- Volunteers
- 152 people
- Sponsor
- Skane University Hospital
Incisional Hernia of Midline of Abdomen
Open Vs. Endoscopic Transversus Abdominis Release Trial
This study aims to comparatively evaluate the early and long-term results of open and endoscopic TAR procedure for large midline incisional ventral hernias.
- Trial name
- NCT06195332
- Testing
- open TAR, endoscopic TAR
- Where
- Russia
- Volunteers
- 36 people
- Sponsor
- City Clinical Hospital No.1 named after N.I. Pirogov
Ventral Hernia, Incisional Hernia
A Prospective, Multicenter All Comers Study of Phasix Mesh for Ventral or Incisional Hernia Repair
Collect data on safety, performance, and effectiveness of Phasix Mesh in subject requiring primary ventral and incisional hernias.
- Trial name
- NCT02053168
- Testing
- Resorbable Mesh
- Where
- 6 sites in United States
- Volunteers
- 33 people
- Sponsor
- C. R. Bard
Incisional Hernia After Midline Laparotomy, Quality of Life (QOL)
NoPro - Norwegian Hernia Prophylaxis Study
A multicenter randomized controlled trial comparing midline laparotomy closures using the small-bite suture technique alone to those using the small-bite suture technique with an additional onlay prophylactic polypropylene mesh.
- Conditions
- Incisional Hernia After Midline Laparotomy, Quality of Life (QOL), Burst Abdomen, Surgical Site Infections
- Trial name
- NoPro (NCT06858020)
- Testing
- Prophylactic polypropylene onlay mesh
- Where
- Norway
- Volunteers
- 150 people
- Sponsor
- Sykehuset Innlandet HF
Ventral Hernia
Repair of Large Incisional Hernias - To Drain or Not to Drain Randomised Clinical Trial
The aim of this study was to perform a randomised clinical trial comparing the use of closed-suction tubular drains and progressive tension sutures in individuals with large incisional hernias subjected to onlay mesh repair to…
- Trial name
- NCT02163460
- Testing
- Drain, Progressive Tension Sutures
- Where
- Brazil
- Volunteers
- 42 people, healthy volunteers welcome
- Sponsor
- Universidade Estadual do Oeste do Paraná
Hernia Incisional, Suture, Complication
DuraMesh Laparotomy Closure Following Trauma and Emergency Surgery
The proposed project aims to evaluate the safety of DuraMesh™ suture for laparotomy closure in an emergent setting, while also providing preliminary efficacy data with regard to incisional hernia prevention.
- Trial name
- NCT04312165
- Testing
- Duramesh Laparotomy Closure, Conventional suture closure
- Where
- 2 sites in United States
- Sponsor
- Uniformed Services University of the Health Sciences
Incisional Hernia, Onlay Mesh
Incisional Hernia Repair by Abdominal Wall Component Release With Contemporary Onlay Mesh Fixation
There is a great expansion in the presentation of complex incisional hernia defects. Primary closure for most cases is impossible with a high rate of recurrence.
- Conditions
- Incisional Hernia, Onlay Mesh, Abdominal Wall Component Release
- Trial name
- NCT06178965
- Testing
- Incisional Hernia Repair by Abdominal Wall Component Release with Contemporary Onlay Mesh Fixation
- Where
- Egypt
- Volunteers
- 17 people, healthy volunteers welcome
- Sponsor
- Zagazig University
Hernia, Abdominal, Hernia Incisional
Outcomes of Trasversus Abdominis Release for Complex Abdominal Wall Hernia
This multicenter retrospective study analyzed data from 308 patients who underwent open Posterior Component separation with Trasversus release for primary or recurrent complex abdominal hernias between 2015 and 2020.
- Trial name
- IMPACT (NCT06111287)
- Where
- 2 sites in Italy
- Volunteers
- 432 people
- Sponsor
- Azienda Sanitaria Locale Napoli 2 Nord