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Safety and Performance of the OTTAVA System in Participants Undergoing Inguinal Hernia Repair
Sponsor: Auris Health, Inc.
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
Conditions
Interventions
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