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RECRUITING
NCT07298317
NA

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

Sponsor: Auris Health, Inc.

View on ClinicalTrials.gov

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).

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

Key Details

Gender

All

Age Range

22 Years - Any

Study Type

INTERVENTIONAL

Enrollment

30

Start Date

2026-03-11

Completion Date

2026-08-01

Last Updated

2026-08-04

Healthy Volunteers

No

Interventions

DEVICE

OTTAVA Robotic System

Participants will undergo the IHR procedure using OTTAVA Robotic System.

Locations (4)

Tampa General Hospital

Tampa, Florida, United States

Indiana University North Hospital

Carmel, Indiana, United States

Duke Regional Hospital

Durham, North Carolina, United States

The University of Texas Health Science Center at Houston

Houston, Texas, United States