Safety and Performance of the OTTAVA System in Participants Undergoing Inguinal Hernia Repair
NCT07298317 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30
Last updated 2026-08-04
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).
Conditions
- Hernia, Inguinal
Interventions
- DEVICE
-
OTTAVA Robotic System
Participants will undergo the IHR procedure using OTTAVA Robotic System.
Sponsors & Collaborators
-
Auris Health, Inc.
lead INDUSTRY
Principal Investigators
-
Auris Health, Inc. Clinical Trial · Auris Health, Inc.
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 22 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2026-03-11
- Primary Completion
- 2026-08-01
- Completion
- 2026-08-01
- FDA Device
- Yes
Countries
- United States
Study Locations
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