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A Prospective Evaluation of Pain After Non-complex Ventral Hernia Repair — ASPIRE  

Ventral Hernia Clinical Trial

Official title:
ASPIRE: A proSpective Evaluation of PaIn After Non-complex ventRal hErnia Repair

Clinical Trial Summary

The study aims to evaluate outcomes relating to pain and QOL after robotic-assisted or laparoscopic non-complex ventral hernia repair.

Clinical Trial Description

This is a prospective, observational, study across robotic-assisted and laparoscopic primary (non-recurrent) umbilical and incisional hernia repair. The study aims to evaluate pain and QOL outcomes through 30 days. During the post-operative period through 30 days, pain medication intake, subject reported pain and quality of life 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 NCT04855227
Study type Observational
Source Intuitive Surgical
Contact Smruthi Srinivasa Murthy, MS
Phone 682-552-6131
Email smruthi.srinivasamurthy@intusurg.com
Status Recruiting
Phase
Start date August 31, 2021
Completion date December 2025
View Details
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