Status: Recruiting
Safety and Performance of the OTTAVA System in Participants Undergoing Inguinal Hernia Repair
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).
Participants needed: 30
Trial details
Age: 22+Biological sex: AllType: InterventionalSponsor: Auris Health, Inc.Updated: Aug 4, 2026Locations: 4
Eligibility criteria
Willing and able to provide informed consent [+4]
Physician determination, including intraoperative finding, that subject is a poo... [+8]