Home › NCT07181876
Robotic Minimally Invasive Inguinal Hernia Repair Post-Market Clinical Study With the DEXTER Robotic System
RecruitingObservational study
Who can join
Ages 22 and older · All sexes
Full eligibility criteria
Inclusion Criteria: * 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 Exclusion Criteria: * 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
About the study
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.
What is being tested
- inguinal hernia repair (device)
Sponsor: Distalmotion SA · Participants: 140 · Started: Nov 26, 2025
Contact the study team
- Pascal Lehmann · Phone: +41215105890
Official record on ClinicalTrials.gov — NCT07181876
Locations in the U.S.
| New York | Northtowns Ambulatory Surgical Center (NASC), Buffalo |
| Texas | Memorial Hermann-Texas Medical Center - UT Health Houston, Houston |
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.