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Robotic Minimally Invasive Inguinal Hernia Repair Post-Market Clinical Study With the DEXTER Robotic System | Clinical Trials | Clareo Health

RECRUITING

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

NCT07181876•Distalmotion SA

View on ClinicalTrials.gov

Summary

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.

Eligibility

Age

22 - No limit years

Sex

ALL

Healthy Volunteers

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

Locations (2)

Northtowns Ambulatory Surgical Center (NASC)

Buffalo, New York, United States

Memorial Hermann-Texas Medical Center - UT Health Houston

Houston, Texas, United States

Key Dates

Start Date

November 26, 2025

Primary Completion Date

December 1, 2028

Completion Date

December 1, 2029

Last Updated

January 22, 2026

Enrollment

140

ESTIMATED participants

Conditions

Inguinal Hernia Repair

Interventions

inguinal hernia repair

DEVICE

Contacts

Pascal Lehmann

CONTACT

+41215105890 pascal.lehmann@distalmotion.com

Transversalis Fascia Plane Block for Laparoscopic Inguinal Hernia Repair

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ACTIVE_NOT_RECRUITINGNA

Laparoscopic Inguinal Hernia Repair TEP vs TAPP

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NOT_YET_RECRUITINGNA

Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: January 22, 2026Data synced to Clareo: March 29, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

View ClinicalTrials.gov Terms and Conditions

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

Inclusion Criteria

Exclusion Criteria

Transversalis Fascia Plane Block for Laparoscopic Inguinal Hernia Repair

Laparoscopic Inguinal Hernia Repair TEP vs TAPP

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Emergency Hernia Repair

The Effects of Abdominal Plane Blocks on Postoperative Quality of Recovery

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