Clinical trials: Ventral Hernias
Ventral Hernia Repair
ORION Study: Mesh Position and Risk During Subsequent Minimally Invasive Abdominal Surgery
Ventral hernia repair is one of the most commonly performed abdominal surgical procedures worldwide, increasingly carried out using minimally invasive techniques.
- Trial name
- ORION (NCT07384962)
- Where
- Italy
- Volunteers
- 790 people
- Sponsor
- Istituto Auxologico Italiano
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
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, 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
Ventral Hernia
Investigating the Feasibility and Outcomes of Patient Self-Drain Removal After Ventral Hernia Repair
The goal of this randomized controlled trial is to teach patients to safely and effectively self-remove drains at home in adults (aged 18 and older) following a ventral hernia repair (VHR).
- Trial name
- SDR (NCT06237855)
- Testing
- Self-drain removal
- Where
- United States
- Volunteers
- 11 people
- Sponsor
- Wake Forest University Health Sciences
Hernia, Ventral
Pain and Readmission After Lap IPOM vs. Robotic Ventral Hernia Repair
Comparison of results after rTARUP and lap IPOM in patients with small- and medium-sized ventral hernia. Retrospective cohort study of consecutive patients undergoing rTARUP or IPOM repair for small or medium-sized primary…
- Trial name
- NCT05320055
- Testing
- robotic repair
- Where
- Denmark
- Volunteers
- 59 people
- Sponsor
- Bispebjerg Hospital
Umbilical Hernia
The Flemish Umbilical Nitinol Mesh Trial, a Multicenter Trial
The use of mesh in the repair of umbilical hernias is a gold standard. The best location of the mesh remains a matter of discussion, i.e.
- Trial name
- FUN (NCT01543789)
- Testing
- Intraperitoneal mesh placement, Preperitoneal mesh placement
- Where
- 3 sites in Belgium
- Volunteers
- 44 people
- Sponsor
- University Hospital, Ghent
Umbilical Hernia
Analgesic Efficacy After Umbilical Hernia Repair in Children
Umbilical hernia repair is a common painful outpatient procedure performed in children. Often analgesia for this procedure is provided by using local infiltration of the surgical site by the surgeons and perioperative opioids and…
- Trial name
- NCT00578136
- Testing
- Bupivacaine
- Where
- United States
- Volunteers
- 52 people
- Sponsor
- Children's Hospital of Philadelphia
Ventral Incisional Hernia
Observational Biologic or Prosthetic Mesh
The purpose of this study is to assess the incidence of hernia recurrence with the use of biologic and prosthetic mesh in ventral hernia repair.
- Trial name
- NCT03317665
- Testing
- Mesh for hernia repair
- Where
- 3 sites in United States
- Volunteers
- 28 people
- Sponsor
- University of South Florida
Incisional Hernia Repair, Ventral Hernia Repair
Comparative Evaluation of Preoperative Preparation Methods in Patients With Large Incisional Hernias
Patients with large, complex, or giant incisional hernias often require advanced preoperative optimization to facilitate safe abdominal wall reconstruction and reduce postoperative complications.
- Trial name
- AWR-PREP (NCT07549113)
- Testing
- Botulinum Toxin A (Botox ), Progressive Preoperative Pneumoperitoneum, Combined Preoperative Preparation
- Where
- Russia
- Volunteers
- 120 people
- Sponsor
- State Budget Public Health Institution Scientific Research Institute - Ochapovsky Regional Clinical Hospital
Ventral Hernia, Panniculus
Effect of Prehabilitation on Surgical Outcomes of Abdominally-based Plastic Surgery Procedures
The purpose of this study is to determine whether a program to optimize patient physical fitness and nutrition ("prehabilitation") prior to and after plastic surgery involving the abdomen improves surgical outcomes.
- Conditions
- Ventral Hernia, Panniculus, Abdominoplasty, Flap Reconstruction
- Trial name
- NCT04787874
- Testing
- Prehabilitation Program
- Where
- 2 sites in United States
- Volunteers
- 520 people, healthy volunteers welcome
- Sponsor
- Stanford University