Robotic Minimally Invasive Inguinal Hernia Repair Post-Market Clinical Study With the DEXTER Robotic System
Recruiting now
Conditions studied: Inguinal Hernia Repair
In brief
The purpose of this post-market, observational study is to collect data under anticipated conditions of use that demonstrates that DEXTER performs as intended in the intended patient population, including a variety of representative disease etiologies and demographic groups.
Key facts
- Study ID
- NCT07181876
- Run by
- Distalmotion SA
- People needed
- 140
- Starts
- 2025-11-26
- Expected to finish
- 2029-12-01
- Last updated by the study team
- 2026-07-06
Who can join
Age: 22 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Subject is ≥ 22 years of age at time of enrollment/consent
- Subject is indicated for and planned to undergo robot-assisted and laparoscopic surgery for unilateral or bilateral inguinal hernia repair
- Subject is able and willing to comply with the protocol requirements, has been informed of the nature of the study, and has signed the IRB-approved informed consent form
You may not qualify if…
- Subject with any relative and absolute contraindications for the use of conventional endoscopes and endoscopic surgical instruments and/or general non-procedure specific contraindications to endoscopic surgery including bleeding diathesis and pregnancy
- Subject is participating in another clinical investigation at the time of enrollment or planned participation at any time during this clinical study
- Subject has a known or suspected medical condition that, in the opinion of the Investigator, may put the subject at risk for participation in this clinical study
Where it is running
- Northtowns Ambulatory Surgical Center (NASC) — Buffalo, New York, United States (enrolling)
- Memorial Hermann-Texas Medical Center - UT Health Houston — Houston, Texas, United States (enrolling)
Full record on ClinicalTrials.gov
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