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● Recruiting
Safety and Performance of the OTTAVA System in Participants Undergoing Inguinal Hernia Repair
Condition: Hernia, Inguinal · Sponsor: Auris Health, Inc.
About this study
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).
This description comes directly from the study's public registry record.
Talk to the study team
Damaris Pederson, MPH · 1 619 708 2607 · Dpeders@its.jnj.com
Dominic Papandria, MD · 16509226723 · DPapandr@ITS.JNJ.com
Always discuss trial participation with your own doctor first.
Locations (4)
| Tampa General Hospital | Tampa, Florida, United States | Recruiting |
| Indiana University North Hospital | Carmel, Indiana, United States | Recruiting |
| Duke Regional Hospital | Durham, North Carolina, United States | Recruiting |
| The University of Texas Health Science Center at Houston | Houston, Texas, United States | Recruiting |
Sponsor or site team? See the site landscape for this trial — listed sites, countries, and recruiting-density context.
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Source record: clinicaltrials.gov/study/NCT07298317