Robotic Minimally Invasive Inguinal Hernia Repair Post-Market Clinical Study With the DEXTER Robotic System

Part of paid clinical trials in Buffalo, New York.

Sponsor
Distalmotion SA
Study ID
NCT07181876
Status
Recruiting
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Conditions

  • Inguinal Hernia Repair

Eligibility Criteria

Sex
ALL
Age
22 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • inguinal hernia repair — DEVICE
    Robotic-assisted inguinal hernia repair with the DEXTER robotic surgery system

Study Details

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 Dates

Start date
Nov 26, 2025
Status verified
Jan 2026
Primary completion
Dec 31, 2028
Completion
Dec 31, 2029

Study Design

Enrollment
140 participants (estimated)

Primary Outcome Measure

Primary safety outcome [ Time Frame: up to 30 days after surgery ]

Central Contacts

Locations (2)

FacilityCityStateZIPSite coordinators
Northtowns Ambulatory Surgical Center (NASC)BuffaloNew York14221-
Memorial Hermann-Texas Medical Center - UT Health HoustonHoustonTexas77030
Julie Holihan, MD
[email protected]
+1 (713) 486-1330

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By research site
Northtowns Ambulatory Surgical Center (NASC)· Buffalo, NYMemorial Hermann-Texas Medical Center - UT Health Houston· Houston, TX

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