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.
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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

Damaris Pederson, MPH

1 619 708 2607

Dpeders@its.jnj.com

CONTACT

Dominic Papandria, MD

16509226723

DPapandr@ITS.JNJ.com

CONTACT