Clinical trials: Hernia, Ventral
Ventral Hernia
A Prospective, Observational Study Utilizing Phasix™ Mesh During Ventral and Incisional Hernia Repair Surgery
The objective of this study is to collect efficacy, safety and utility data with Phasix™ Mesh in ventral and incisional repair procedures by evaluating the following: 1.
- Trial name
- NCT01863030
- Testing
- Phasix mesh implant
- Where
- United States
- Volunteers
- 31 people
- Sponsor
- John Roth
Open Midline Laparotomy
Prophylactic Reinforcement of Ventral Abdominal Incisions Trial
This trial is being conducted to evaluate the efficacy of Phasix™ Mesh implantation at the time of midline fascial closure compared to primary suture closure in preventing a subsequent incisional hernia in subjects at risk for…
- Trial name
- PREVENT (NCT03911700)
- Testing
- Phasix™ Mesh
- Where
- 32 sites in United States, Austria and 3 more
- Volunteers
- 477 people
- Sponsor
- C. R. Bard
Incisional Ventral Hernia
Cytokine Response to Abdominal Wall Reconstruction
This is a prospective, observational translational study of patients undergoing major abdominal wall reconstruction with primary fascial closure.
- Trial name
- NCT07422584
- Testing
- Not applicable- observational study
- Where
- United States
- Volunteers
- 25 people, healthy volunteers welcome
- Sponsor
- Northwestern University
Incisional Hernia, Ventral Hernia
Watchful Waiting of Incisional Hernias
This study is being conducted to gain a better understanding of the quality of life for patients with a diagnosis of primary and recurrent incisional hernias and 1) who decline to have surgery to repair the hernia or 2) patients…
- Conditions
- Incisional Hernia, Ventral Hernia, Umbilical Hernia
- Trial name
- NCT00351455
- Testing
- smoking cessation, tighter diabetic control, diet and exercise program
- Where
- United States
- Volunteers
- 50 people
- Sponsor
- Baylor College of Medicine
Ventral Hernia, Liver Transplantation
Ventral Hernia Prevention After Liver Transplantation
This study aims to evaluate if the risk of developing ventral hernia after liver transplantation can be reduced through the prophylactic implantation of a synthetic, fully resorbable mesh "Phasix" in the course of liver…
- Trial name
- NCT03222102
- Testing
- Phasix mesh
- Where
- Austria
- Volunteers
- 36 people
- Sponsor
- Medical University of Graz
Incisional Ventral Hernia, Recurrent Ventral Hernia
Modified "Open Intraperitoneal Mesh" Technique of Incisional Ventral Hernia Repair
Ventral hernias, primary and recurrent, are major surgical challenge. We aim to investigate efficacy of modified technique of ventral hernias repair: an "open intraperitoneal mesh" technique.
- Trial name
- NCT01953302
- Testing
- modified "open mesh technique"
- Where
- Croatia
- Volunteers
- 124 people
- Sponsor
- Varazdin General Hospital
Ventral Hernia
Outpatient Repair of Small Reducible Ventral Hernias Using Local Anesthesia: A Pilot Study
Primary midline hernias, including umbilical and epigastric hernias, are prevalent surgical conditions, necessitating intervention.
- Trial name
- OPD-repair (NCT07514273)
- Testing
- Repair of small ventral hernia under lokal anesthesia, Hernia Repair, OPD Repair
- Where
- Sweden
- Volunteers
- 35 people
- Sponsor
- Region Örebro County
Ventral Hernia
Biological Meshes in Infected Fields: a Randomized Controlled Trial
The SIMBIOSE trial is a large multicenter phase III prospective randomized controlled single blinded trial comparing the use of biological mesh versus traditional wound care without biological mesh in patients with an infected…
- Trial name
- SIMBIOSE (NCT01594450)
- Testing
- Biological mesh, without biological mesh
- Where
- France
- Volunteers
- 110 people
- Sponsor
- University Hospital, Lille
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
Data Agreement Between a Database and Hospital Files After a Ventral Hernia Repair
High Agreement Between the Danish Ventral Hernia Database and Hospital Files in Region Zealand
Is there agreement between data in the Danish Ventral Hernia Database and patient files
- Trial name
- NCT01827410
- Testing
- Ventral hernia repair
- Where
- Denmark
- Volunteers
- 408 people
- Sponsor
- Zealand University Hospital
Frailty, Ventral Hernia
Targeted Prehabilitation With Physical Exercise and Inspiratory Muscle Training for Elderly Frail Patients Prior to Ventral Hernia Repair
The purpose of this study is to assess the physical fitness of patients undergoing hernia repair and correlate the postoperative outcomes and recovery as well as assess the impact of a targeted physical exercise program…
- Trial name
- NCT06874413
- Testing
- Prehabilitation, Standard of Care (SOC)
- Where
- United States
- Volunteers
- 120 people
- Sponsor
- Prisma Health-Upstate
Cirrhosis, Umbilical Hernia
Elective Umbilical Hernia Repair in Patients With Cirrhosis
Liver cirrhosis is a frequent and severe chronic disease. About 20 % of patients with liver cirrhosis develop umbilical hernias. In comparison, the prevalence in the general population is around 2 %.
- Trial name
- NCT04687579
- Testing
- Screening, Preoperative optimization, Umbilical hernia repair
- Volunteers
- 51 people
- Sponsor
- Hvidovre University Hospital
Ventral Hernia
A Clinical Trial Using Spy Elite System in Planning Tissue Advancement Flaps After Ventral Hernia Repair
The purpose of this project is to assess the efficacy of the Spy Elite System (LifeCell Corporation, Branchburg, NJ, USA) in planning tissue advancement flaps and reducing wound complications after complex ventral hernia repairs.
- Trial name
- NCT01886963
- Testing
- SPY - Unblinded use of SPY Elite, Control - Blinded use of SPY Elite
- Where
- United States
- Volunteers
- 115 people
- Sponsor
- Wake Forest University Health Sciences
Hernia, Ventral, Hernia, Abdominal
Abdominal Wall Tension in Patients Undergoing Ventral Hernia Repair Without Component Separation
The purpose of this study is to use a scale to learn more about the tension of the abdominal wall in hernia repairs without component separation. 1.
- Conditions
- Hernia, Ventral, Hernia, Abdominal, Hernia Abdominal Wall
- Trial name
- NCT06051578
- Testing
- Abdominal wall tension measurement
- Where
- United States
- Volunteers
- 50 people, healthy volunteers welcome
- Sponsor
- The Cleveland Clinic
Abdominal Wall Hernia
Clinical Study of Hernia Ring Closure Method in Laparoscopic Abdominal Wall Hernia Repair
By comparing the time of closing the hernia ring, the degree of pain, and the recovery of gastrointestinal tract in different groups Intervening, infection, recurrence and medical cost, to find out whether patients with abdominal…
- Trial name
- NCT05661097
- Testing
- Suture mode
- Where
- China
- Volunteers
- 100 people
- Sponsor
- Bo Li
Incisional Hernia Repair, Ventral Incisional Hernia
Standard Closure vs. Integrated Mesh-Fascial Closure (IMFC) for Incisional Hernia Repair
This study compares two surgical techniques for closing the abdominal wall in adult patients who have an incisional hernia (a weakness or opening in a previous surgical incision) or who require prophylactic mesh placement during…
- Trial name
- IMFC (NCT07843225)
- Testing
- Integrated Mesh-Fascial Closure, Standard Fascial Closure with Mesh
- Where
- Argentina
- Volunteers
- 60 people
- Sponsor
- Hospital Zonal General De Agudos Mario V Larrain
Ventral Hernia
Biologic Mesh Versus Synthetic Mesh in Repair of Ventral Hernias
This study will compare the safety, efficacy and cost effectiveness of a permanent synthetic mesh versus a biologic prosthesis for the repair of ventral hernias in the setting of clean-contaminated (Class 2) or contaminated…
- Trial name
- NCT02451176
- Testing
- Davol Bard Soft Mesh synthetic, LifeCell Strattice Reconstructive Tissue Biologic
- Where
- 4 sites in United States
- Volunteers
- 253 people
- Sponsor
- Michael Rosen
Ileus
A Study Evaluating Intravenous (IV) MOA-728 for the Treatment of Postoperative Ileus (POI) in Participants After Ventral Hernia Repair
This study will evaluate the safety and efficacy of two different dose regimens (12 milligrams [mg] and 24 mg) of IV MOA-728 versus placebo in shortening the time to return of bowel function in participants receiving opioid…
- Trial name
- NCT00528970
- Testing
- MOA-728
- Where
- 106 sites in United States, Australia and 9 more
- Volunteers
- 374 people
- Sponsor
- Bausch Health Americas, Inc.
Hernia Abdominal Wall, Botox Injection
Preoperative BOTOX® Injection for Large Ventral Hernia Repair
This study is for adults who need open surgery to repair a very large abdominal (ventral) hernia. This study tests whether a one-time, image-guided injection of a medicine commonly known as "BOTOX®" (onabotulinumtoxinA) into the…
- Conditions
- Hernia Abdominal Wall, Botox Injection, Hernia Incisional Ventral, Hernia Repair With Compartment Syndrome
- Trial name
- PRETOX (NCT07220382)
- Testing
- OnabotulinumtoxinA Injection, OnabotulinumtoxinA, 0.9 % Normal Saline
- Where
- United States
- Volunteers
- 188 people
- Sponsor
- The Cleveland Clinic
Hernia, Ventral, Laparoscopy
Peritoneal Bridging in Laparoscopic Ventral Hernia Repair
Laparoscopic ventral hernia repair (VHR) is usually performed by reducing the contents in the hernia sac from the abdominal cavity and then covering the defect from the inside with a mesh, i.e. Intraperitoneal Onlay Mesh (IPOM).
- Conditions
- Hernia, Ventral, Laparoscopy, Seroma
- Trial name
- BriClo (NCT03344575)
- Testing
- Conventional defect closure, Peritoneal bridging
- Where
- Sweden
- Volunteers
- 50 people
- Sponsor
- Karolinska Institutet