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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


NCT number NCT04855227
Study type Observational
Source Intuitive Surgical
Contact Jennifer Mueller, MBT
Phone 510-552-9880
Email [email protected]
Status Not yet recruiting
Phase
Start date April 2021
Completion date November 2022

See also
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