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Pain and Quality of Life After Retromuscular Ventral Hernia Repair (RECOVER) — RECOVER  

Ventral Hernia Clinical Trial

Official title:
RECOVER: a pRospECtive evaluatiOn of Pain After Retromuscular VEntRal Hernia Repair

Clinical Trial Summary

The study aims to explore the difference in outcomes relating to pain and quality of life after open, laparoscopic, and robotic-assisted retromuscular ventral hernia repair.

Clinical Trial Description

This is a prospective, multicenter, observational study assessing outcomes relating to pain and quality of life for subjects undergoing open, laparoscopic, or robotic-assisted retromuscular ventral hernia repair. The study will focus on short-term post-operative outcomes through 3 months. The study will also collect recurrence data through 1 year. During the post-operative period through 3 months, pain medication intake, subject reported pain (on post-operative day 7, 14, 21, 28, and 3 months) and quality of life (on day 28, 3 months, and 1 year) and incidence of intra-operative and post-operative adverse events related to the ventral hernia repair will be collected. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04487522
Study type Observational
Source Intuitive Surgical
Contact Jennifer Mueller
Phone 15105529880
Email jennifer.mueller@intusurg.com
Status Recruiting
Phase
Start date July 16, 2020
Completion date December 1, 2024
View Details
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