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

NCT07181876 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 140

Last updated 2026-01-22

No results posted yet for this study

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.

Conditions

  • Inguinal Hernia Repair

Interventions

DEVICE

inguinal hernia repair

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

Sponsors & Collaborators

  • Veranex, Inc.

    collaborator UNKNOWN

  • Distalmotion SA

    lead INDUSTRY

Eligibility

Min Age
22 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-11-26
Primary Completion
2028-12-31
Completion
2029-12-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07181876 on ClinicalTrials.gov