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Laparoscopic vs. Robotic Ventral Hernia Repair With IPOM
NCT03283982 · The Cleveland Clinic · Updated 25 July 2022
- What is being tested
- Robotic Ventral Hernia Repair with IPOM; Laparoscopic Ventral Hernia Repair with IPOM
- For
- Ventral Hernia
- Kind of study
- Tests a treatment or device on volunteers. No drug phase (a device or procedure study).
- Who can join
- Ages 18 years and older. About 75 people. The full rules are on the registry page.
- Where
- United States
- When
- Starts or started 11 Sept 2017, ends 31 Jan 2021. Registered 15 Sept 2017.
- Results
- Posted on the registry on 19 July 2022.
In the researchers' words
The investigators aim to conduct a registry-based, randomized controlled trial to investigate if the robotic platform for minimally invasive ventral hernia repair with intraperitoneal onlay mesh (IPOM), when compared to the laparoscopic platform, will influence on early postoperative pain scores, wound morbidity (surgical site infections, surgical site occurrences and surgical site occurrences requiring procedural intervention), ventral hernia recurrence rate and abdominal wall-specific quality of life.
Sites
- Cleveland Clinic Comprehensive Hernia CenterCleveland, Ohio, United States