Clinical trials: Hernia, Incisional
Ventral Hernia
Longitudinal Relaxing Incision as a Technique for Recurrence Prevention in Ventral Hernia
The aim of the study is showing the efficiency of using Longitudinal relaxing incision as a Technique for recurrence prevention in Ventral Hernia
- Trial name
- NCT05526209
- Testing
- using longitudinal relaxing incision as a technique for recurrence prevention in ventral hernia
- Volunteers
- 40 people
- Sponsor
- Assiut University
Ventral Hernia, Ventral Incisional Hernia
The IMPACT Study: Personalized Physical Therapy for Better Recovery and a Stronger Core After Hernia Surgery
Ventral hernia repair is among the most common operations performed in the United States each year, yet the great majority of patients receive no structured rehabilitation for the persistent pain, weakness, and functional loss…
- Conditions
- Ventral Hernia, Ventral Incisional Hernia, Post Operative Pain
- Trial name
- IMPACT (NCT07145099)
- Testing
- PT Group, Usual Care
- Where
- United States
- Volunteers
- 60 people
- Sponsor
- Thomas Jefferson University
Hernia Incisional Ventral
Management Of Large Incisional Hernia, Double Mesh Modification Of Chevrel's Technique Versus On Lay Mesh Hernioplasty
comparison between two groups of large midline incisional hernia, the first group managed by double mesh modification of chevrel's technique the second one managed by conventional onlay mesh repair
- Trial name
- NCT04430816
- Testing
- double mesh modification of chevrel's technique, on lay mesh hernioplasty
- Where
- Egypt
- Volunteers
- 43 people
- Sponsor
- Zagazig University
Incisional Hernia
A Prospective, Double-Blinded, Randomized Controlled Trial of dHACM for Incisional Hernia Prophylaxis
Currently, no standard of care exists to prevent incisional hernias (IH). This study will compare how frequently IH develop in standard abdominal closures vs. abdominal closures with dHACM added.
- Trial name
- NO-HERNIA (NCT04417140)
- Testing
- dHACM (AmnioWrap)
- Where
- United States
- Volunteers
- 533 people, healthy volunteers welcome
- Sponsor
- Louisiana State University Health Sciences Center in New Orleans
Incisional Hernia
Trocar Site Incisional Hernia Prevention
Objective: To test the preventive effect of the placement of an onlay mesh versus the use of a fascial closure device at the umbilical trocar site closure in order to prevent incisional hernia after laparoscopic surgery.
- Trial name
- PHIT (NCT04699201)
- Testing
- Hincisional hernia prevention by onlay prosthesis trocar closure, laparoscopic cholecystectomy, Abdominal ultrasound
- Where
- 2 sites in Spain
- Volunteers
- 94 people, healthy volunteers welcome
- Sponsor
- Hospital Universitari Joan XXIII de Tarragona.
Incisional Hernia/Prevention and Control
Prometheus: Prophylactic Mesh After OLtx for Hernia Reduction Study.
A multicenter prospective, consecutive case series study, on the use of a bio-absorbable mesh for prevention of incisional hernia, in high risk patients, after orthotopic liver transplantation.
- Trial name
- PROMETHEUS (NCT07744230)
- Testing
- mesh
- Where
- Italy
- Volunteers
- 100 people
- Sponsor
- University of Rome Tor Vergata
Ventral/Incisional Hernia Repairs
Trunk Strength Study
The purpose of this study is to measure abdominal wall strength both preoperatively and postoperatively in patients undergoing ventral/incisional hernia repairs.
- Trial name
- NCT01300936
- Where
- United States
- Volunteers
- 10 people
- Sponsor
- University of Kentucky
Hernia Recurrence Post Laparoscopic Incisional Hernia Repair in Liver Transplant Versus Non-transplant Patients.
Laparoscopic Incisional Hernia Repair in Liver Transplant Patients
Retrospective analysis of patients undergoing laparoscopic incisional hernia repair. Study group: Patients with incisional hernia post liver transplantation Control group: Patients with incisional hernia post any other laparotomy…
- Trial name
- NCT02123719
- Testing
- Surgery
- Where
- Austria
- Volunteers
- 112 people
- Sponsor
- Medical University Innsbruck
Mesh
Lumber Hernia Repair Using Sandwich Mesh Technique
Lumbar incisional hernia occurs after lumbar incision which is difficult to manage due deficient fascial aponeurosis and a proximity of the bonny boundaries, namely the iliac crest and the last rib.
- Trial name
- NCT07196254
- Testing
- sandwich mesh technique
- Where
- Egypt
- Volunteers
- 10 people
- Sponsor
- Zagazig University
Incisional Hernia
ProGripTM Self-Gripping Polyester Mesh in Incisional Hernia Prevention
Interventional, prospective, multicenter, post-marketing clinical follow-up study. After midline laparotomy, the probability to develop an incisional hernia ranges from 10% to 50% depending on the complexity of the surgery and…
- Trial name
- POETRY (NCT03912662)
- Testing
- Mesh augmented reinforcement
- Where
- 11 sites in France
- Volunteers
- 32 people
- Sponsor
- Medtronic - MITG
Incisional Hernia, Recurrent Hernia
Pulmonary Ventilation Function Between Patients With Primary and Recurrent Incisional Hernia: a Cross-sectional Study
Purpose Chronic obstructive pulmonary disease (COPD) is a risk factor for incisional hernia, COPD has persistent airflow restriction and pulmonary ventilation dysfunction.
- Conditions
- Incisional Hernia, Recurrent Hernia, COPD, Pulmonary Ventilation Function
- Trial name
- NCT05991024
- Testing
- the incisional hernia recurrent
- Where
- China
- Volunteers
- 164 people
- Sponsor
- Fudan University
Incisional Hernia
Xen Matrix™ AB Surgical Graft in Ventral or Incisional Midline Hernias
This study aims to prospectively explore the use of XenMatrix™ AB Surgical Graft for ventral or incisional midline hernia repair in patients across all wound classes ("All Comers") through 24 months post repair.
- Trial name
- NCT02691962
- Testing
- Xen Matrix AB
- Where
- 11 sites in United States
- Volunteers
- 75 people
- Sponsor
- C. R. Bard
Hernia, Incisional
MRI Imaging of Ipsilateral Retromuscular Access
The aim of this study is to measure the mesh shrinkage and the visualization of the mesh with MRI scan at 1 month and 13 months after robot assisted retromuscular incisional hernia repair with ipsilateral access and the use of…
- Trial name
- NCT03380312
- Testing
- rTARUP technique
- Where
- Belgium
- Volunteers
- 20 people
- Sponsor
- Filip Muysoms
Lumbar Disc Herniation, Degenerative Disc Disease
Peri-Incisional Drug Injection in Lumbar Spine Surgery
This is a randomized prospective study that will compare the use of narcotics in a control group of non-injected patients with a treatment arm of patients injected intra-operatively with a ropivacaine, morphine, and epinephrine…
- Conditions
- Lumbar Disc Herniation, Degenerative Disc Disease, Spondylolisthesis
- Trial name
- NCT03513445
- Testing
- Morphine, Epinephrine, naropin
- Where
- United States
- Sponsor
- University of Minnesota
Incisional Hernia
Usefulness of a Prothetic Absorbable Mesh in Incisional Hernia Prevention After Midline Laparotomy
Background: Development of an incisional hernia is one of the most frequent complications of midline laparotomies requiring reoperation.
- Trial name
- PREBIOUS (NCT02208557)
- Testing
- Reinforcement with Absorbable Mesh, Control CT, Clinical Follow Up
- Where
- 6 sites in Spain
- Volunteers
- 488 people
- Sponsor
- Hospital Universitari Vall d'Hebron Research Institute
Primary Ventral and Incisional Hernia Repair
Progrip Ventral Study for Sublay Repair
A novel concept of self-gripping mesh has been developed to achieve secure and long-term posterior wall reinforcement. ProGrip™ mesh is a lightweight (40g/m2) monofilament polypropylene or polyester mesh with resorbable…
- Trial name
- NCT01622127
- Testing
- Parietex ProGrip™
- Where
- Belgium
- Volunteers
- 55 people
- Sponsor
- University Hospital, Ghent
Incisional Hernia
Umbilical vs Paraumbilical Trocar Placement in Patients Undergoing Elective Laparoscopic Cholecystectomy
The aim of this study will be to assess the incisional hernia rate of umbilical or paraumbilical port 12 months after laparoscopic cholecystectomy.
- Trial name
- NCT04347642
- Testing
- Umbilical port placement, Paraumbilical port placement
- Where
- 2 sites in Mexico, Spain
- Volunteers
- 180 people
- Sponsor
- Hospital General Universitario Elche
Hernia, Ventral, Ventral Incisional Hernia
Use of Mosquito Net Mesh for Ventral Hernia Repair
It´s a pilot study, randomized, realized in the Central Hospital "Dr. Ignacio Morones Prieto", SLP, Mexico. Hypothesis: The polyethylene mesh is secure in open ventral repair.
- Trial name
- NCT03324854
- Testing
- Rives technique, Drainage, Prophylactic
- Volunteers
- 20 people
- Sponsor
- Hospital Central "Dr. Ignacio Morones Prieto"
Incisional Hernia Occurence
Primary Mesh Closure of Abdominal Midline Wounds
Incisional hernia is the most frequently seen long term complication in surgery causing much morbidity and even mortality in patients.
- Trial name
- PRIMA (NCT00761475)
- Testing
- mesh supported closure, primary closure
- Where
- 12 sites in Austria, Germany and 1 more
- Volunteers
- 480 people
- Sponsor
- Erasmus Medical Center
Incision, Surgical, Suture, Complication
Small Bite Technique Versus Standardised Large Bites Technique in Closure of Midline Laparotomies.
In the attempt to gain quick and complete access to the abdominal regions with the least damage to the nerves and the vascular structures, surgeons use the median laparotomy more frequently.
- Conditions
- Incision, Surgical, Suture, Complication, Incisional Hernia
- Trial name
- SBT-CML (NCT04788875)
- Testing
- Small bite suturing Technique, Standardised Large Bites Technique
- Volunteers
- 108 people
- Sponsor
- Imam Abdulrahman Bin Faisal University