Safety and Performance of the OTTAVA System in Participants Undergoing Inguinal Hernia Repair
Recruiting
N/A
Interventional Study
Hernia, Inguinal
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 22 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 30 (estimated)
- Sponsor
- Auris Health, Inc. · Industry
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About This Trial
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).
Trial Locations
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Eligibility Criteria
Inclusion Criteria
Subjects must satisfy all inclusion criteria to be eligible for enrollment:
1. Willing and able to provide informed consent
2. A minimum of 22 years old at time of consent
3. Scheduled for elective primary inguinal hernia repair
4. American Society of Anesthesiologists (ASA) cla…
Contacts