RecruitingNot ApplicableNCT07298317

Safety and Performance of the OTTAVA System in Participants Undergoing Inguinal Hernia Repair

Technology Evaluation in a Multi-Center Study of Safety and Performance of the OTTAVA System

Sponsor

Auris Health, Inc.

Enrollment

30 participants

Start Date

Mar 11, 2026

Study Type

INTERVENTIONAL

Conditions

Hernia, Inguinal

Summary

The purpose of this study is to assess safety and performance of the OTTAVA System, through 30 days postoperative, in participants undergoing robotic-assisted inguinal hernia repair (IHR).

Eligibility

Min Age: 22 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a medical device called OTTAVA Robotic System for people with hernia, inguinal. The study is currently recruiting participants at 4 locations. People eligible for this study include aged 22 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.