At a glance
ClinicalIndex Comparison RecordStandardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Registry-Based, Prospective, Single-Blind, Randomized Controlled Trial: Robotic vs. Laparoscopic Ventral Hernia Repair With Intraperitoneal Onlay Mesh (IPOM)
In Brief
A clinical study evaluating Robotic Ventral Hernia Repair with IPOM and Laparoscopic Ventral Hernia Repair with IPOM for Ventral Hernia. Completed, enrolled 75 participants across 1 site.
Detailed Summary
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.
Study Details
Timeline
Interventions
Minimally invasive ventral hernia repair with intraperitoneal mesh placement, using the da Vinci robotic platform
Minimally invasive ventral hernia repair with intraperitoneal mesh placement, using the laparoscopic platform