Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Clinical Trial

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

NCT: NCT07298317 · RECRUITING

NCT IDNCT07298317
StatusRECRUITING
Start Date2026-03-11
Completion2026-08-01
SponsorAuris Health, Inc. (INDUSTRY)
First posted
Last updated

Brief 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).

Frequently Asked Questions

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

Safety and Performance of the OTTAVA System in Participants Undergoing Inguinal Hernia Repair is a clinical trial registered under NCT07298317. Current status: RECRUITING.

What is the status of NCT07298317?

The current status of NCT07298317 (Safety and Performance of the OTTAVA System in Participants Undergoing Inguinal Hernia Repair) is: RECRUITING.

When did Safety and Performance of the OTTAVA System in Participants Undergoing Inguinal Hernia Repair start?

Safety and Performance of the OTTAVA System in Participants Undergoing Inguinal Hernia Repair started on 2026-03-11.

Related Devices

K193534Monarch PlatformAuris Health, Inc. K211493Monarch PlatformAuris Health, Inc. K213334Monarch Platform, UrologyAuris Health, Inc. K243219MONARCH™ Platform (MON-000008)Auris Health, Inc. K260382MONARCH™ Platform (MON-000008)Auris Health, Inc.

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

↑