Clinical trials: Hernia Abdominal Wall
Incisional Hernia
Mini- or Less-Open Sublay Operation (MILOS) of Incisional Hernias
Prospective non-randomized observational register study of all elective symptomatic incisional hernias operated on in the Hernia Center of Reference of Gross Sand Hospital using the novel endoscopic assisted Mini- or Less-Open…
- Trial name
- NCT03133000
- Volunteers
- 615 people
- Sponsor
- Gross Sand Hospital
Hernia, Inguinal, Chronic Pain
Nationwide Results on Chronic Pain After Bilateral Transabdominal Preperitoneal Inguinal Hernia Repair (TAPP)
Danish male patients who had undergone bilateral TAPP (July 2012 to June 2013) were recruited from the Danish Hernia Database and cross-checked with hospital files and the National Patient Registry.
- Trial name
- NCT03155230
- Testing
- no intervention
- Where
- Denmark
- Volunteers
- 209 people, healthy volunteers welcome
- Sponsor
- Hvidovre University Hospital
Incisional Hernia, Venous Thromboembolism
Risk Factors of Venous Thromboembolism After Incisional Ventral Hernia Repair.
Aim of our study is to find frequency and risk factors for venous thromboembolism development in patients who underwent surgery for incisional ventral hernia.
- Trial name
- NCT05439187
- Testing
- hernia repair
- Where
- Russia
- Volunteers
- 240 people
- Sponsor
- Pirogov Russian National Research Medical University
Parastomal Hernia
Parastomal Reinforcement With Strattice
The purpose of this study is to compare the clinical outcomes of patients undergoing surgery for a permanent abdominal wall ostomy with and without placement of Strattice fascial inlay, as measured by postoperative occurence of…
- Trial name
- PriSm (NCT00771407)
- Testing
- Strattice Reconstructive Matrix, Standard ostomy creation
- Where
- 23 sites in United States
- Volunteers
- 120 people
- Sponsor
- LifeCell
Inguinal Hernia
Laparoscopic TEP (Total Extra-peritoneal) Repair Vs Open PHS (Prolene Hernia System)
Abdominal wall hernias are common, with a lifetime risk of 27% in men and 3% in women. Inguinal and femoral hernias are the most common affections faced by primary care physicians that require surgical intervention.
- Trial name
- NCT03842852
- Testing
- Inguinal hernia repair
- Where
- Israel
- Volunteers
- 577 people
- Sponsor
- Assuta Medical Center
Urinary Retention, Inguinal Hernia
Study to Prevent Postoperative Urinary Retention
Post-operative urinary retention (POUR) is a common complication after inguinal hernia repair with a reported incidence up 34%. It can be described as the inability to initiate urination or properly empty one's bladder following…
- Trial name
- STOP-POUR (NCT04491526)
- Testing
- TAMSULOSIN Mepha Ret Depocaps 0.4 mg, Control Intervention
- Where
- Switzerland
- Volunteers
- 312 people
- Sponsor
- Antonio Nocito, MD
Abdominal Hernia
Open Versus Robotic-assisted Ventral Hernia Repair, Short and Long-term Outcome
In this randomized clinical trial, the investigators will compare the conventional open repair for hernia in the anterior abdominal wall with the robotic-assisted approach.
- Trial name
- NCT05906017
- Testing
- Open Hernia surgery, Robotic Hernia surgery
- Where
- Denmark
- Volunteers
- 56 people
- Sponsor
- University of Southern Denmark
Hernia, Ventral
Effect of a Preoperative Pulsed Electromagnetic Field and Abdominal Exercises on Muscle Strength Post Ventral Hernioplasty
The aim of this study is to investigate the impact of a preoperative pulsed electromagnetic field and abdominal exercises on muscle strength post ventral hernioplasty.
- Trial name
- NCT05559190
- Testing
- Pulsed electromagnetic field, Graduated abdominal strengthening exercises
- Where
- Egypt
- Volunteers
- 60 people
- Sponsor
- Cairo University
Inguinal Hernia Unilateral, Complications of Surgical Procedures or Medical Care
Desarda Tissue Technique vs Lichtenstein Technique for Primary Inguinal Hernia Repair
This study aims to evaluate whether a surgical technique (Desarda) is superior to the commonly used surgical technique (Lichtenstein) in inguinal hernia repair concerning the occurrence of postoperative complications.
- Trial name
- HP-tis (NCT06650878)
- Testing
- Desarda, Lichtenstein
- Where
- Spain
- Volunteers
- 478 people
- Sponsor
- Consorci Sanitari de l'Alt Penedès i Garraf
Hernia Inguinal, Pain Postoperative
Predictive Factors for the Effectiveness of the Ilioinguinal Iliohypogastric Nerve Block for Hernia Surgery
Inguinal hernia repair is a common surgical procedure done as day surgery. Because patients need to be discharged on the same day, the choice of anesthesia technique is influenced.
- Conditions
- Hernia Inguinal, Pain Postoperative, Regional Anesthesia
- Trial name
- VALI (NCT06121726)
- Testing
- Ilioinguinal-Iliohypogastric nerve block, Local anesthetic
- Where
- Italy
- Volunteers
- 343 people
- Sponsor
- University of Padova
Umbilical Hernia
Randomized Controlled Trial (RCT) Umbilical Hernia Repair (UHR) Absorbable vs Non-absorbable Synthetic Mesh
The goal of this study is to see which of two types of mesh is better for fixing an umbilical hernia. One type of mesh is an absorbable synthetic mesh, which goes away on its own in the body, and the other type of mesh is a…
- Trial name
- NCT05994248
- Testing
- Enform Mesh, Marlex
- Sponsor
- Wake Forest University Health Sciences
Emergency Inguinal Hernia Repair, Emergency Ventral Hernia Repair
Emergency Hernia Repair
Emergency hernia repairs are associated with significantly higher morbidity and mortality compared with elective hernia surgery.
- Trial name
- NCT07314398
- Testing
- Emergency hernia repair
- Volunteers
- 600 people
- Sponsor
- Oulu University Hospital
Inguinal Hernia
Mesh Alone VS Combined Mesh and Darn in the Management of Primary Inguinal Hernia in Adult Males
A prospective randomized study involved 228 individuals with primary inguinal hernia, operated in our departments, between January 2015 to February 2018.
- Trial name
- NCT04891601
- Testing
- polypropelene mesh
- Volunteers
- 228 people, healthy volunteers welcome
- Sponsor
- Jabir Ibn Hayyan Medical University
Hernia, Inguinal, Inguinal Hernia, Direct
Study of Laparoscopic Inguinal Hernia Repair
Although mesh fixation has been associated to an increased incidence of nerve injury and involves increased operative costs, many surgeons feel that fixation is necessary to reduce the risk of hernia recurrence.
- Conditions
- Hernia, Inguinal, Inguinal Hernia, Direct, Inguinal Hernia, Indirect, Hernia, Femoral
- Trial name
- NCT02920307
- Testing
- TEP without fixation, TEP with fixation, TAPP without fixation
- Where
- Turkey (Türkiye)
- Volunteers
- 400 people
- Sponsor
- Medical Park Gaziantep Hospital
HERNIA, VENTRAL
ProLOVE - Prospective Randomized Study of Midline Incisional Hernia Treatment
This purpose of this study is to compare the recovery after an operation of an incisional hernia within the limits of the rectus muscles of the abdominal wall.
- Trial name
- ProLOVE (NCT00472537)
- Testing
- Retromuscular Mesh repair of midline incisional hernia, Laparoscopic repair of midline incisional hernia
- Where
- 7 sites in Sweden
- Volunteers
- 157 people
- Sponsor
- Skane University Hospital
Hernia, Inguinal, Postoperative Complications
Prospective Study Investigating Aspirin and Intraoperative Blood Loss and Complications Following Inguinal Hernia Repair
The purpose of this study is to determine whether aspirin taken in the perioperative period will increase the blood loss associated with open inguinal hernia repairs.
- Conditions
- Hernia, Inguinal, Postoperative Complications, Postoperative Hemorrhage
- Trial name
- NCT02084615
- Testing
- Aspirin
- Where
- United States
- Volunteers
- 300 people
- Sponsor
- Jesse Brown VA Medical Center
Post Abdominal Surgery Pain
A Study Evaluating the Overall Pain Relief and Safety of Intravenous (IV) CR845 in Patients Undergoing Abdominal Surgery
The study schedule is comprised of a 14-day Screening Period, a treatment period and an observation period. All eligible subjects will be randomized into one of 3 treatment groups (1 of 2 dose levels or matched placebo).
- Trial name
- NCT02542384
- Testing
- CR845 IV 1 mcg/kg, CR845 IV 0.5 mcg/kg
- Where
- 23 sites in United States
- Volunteers
- 451 people
- Sponsor
- Cara Therapeutics, Inc.
Inguinal Hernia, Postoperative Pain
Postoperative Effects of TAP Block Versus QLB Type 2 Block
This study compares analgesic effectiveness of transversus abdominis plane block and quadratus lumborum block type 2 in open hernia repair surgery. All of the patients will receive routine intravenous analgesic regimen.
- Trial name
- NCT03126084
- Testing
- Acetaminophen, 0.25% Bupivacaine, 0.5% Bupivacaine+Glucose
- Where
- Turkey (Türkiye)
- Volunteers
- 90 people
- Sponsor
- Bozyaka Training and Research Hospital
Pain
Selective Neurectomy and Mesh Removal for Chronic Postherniotomy Pain
Chronic postherniotomy pain affects every day activities in 5-8% of patients. However, no established treatment for this pain syndrome exists and previous reports on the effect of surgical intervention suffer from methodological…
- Trial name
- NCT00627289
- Where
- 2 sites in Denmark
- Volunteers
- 21 people
- Sponsor
- Copenhagen University Hospital, Rigshospitalet
Seroma, Hernia, Inguinal
Use of Diathermy Versus Blunt Dissection in TEP for Inguinal Hernia
There is a long debate whether monopoloar or blunt dissection should be adopted in TEP to minimise the chance of seroma formation.
- Trial name
- NCT03665883
- Testing
- Monopolar energy, Blunt dissection
- Where
- China
- Volunteers
- 103 people
- Sponsor
- The University of Hong Kong