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Robotic Minimally Invasive Ventral Hernia Repair With DEXTER

NCT07071740 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 33

Last updated 2026-01-22

No results posted yet for this study

Summary

The aim of this clinical investigation is to confirm the perioperative and early postoperative safety and clinical performance (efficacy) of the Dexter Robotic System, in patients undergoing incisional or primary ventral hernia repair.

Conditions

  • Ventral Hernia Repair

Interventions

DEVICE

ventral hernia repair

Robotic-assisted incisional or primary ventral hernia repair with the DEXTER robotic surgery system

Sponsors & Collaborators

  • Confinis

    collaborator INDUSTRY

  • Distalmotion SA

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-06-11
Primary Completion
2026-01-15
Completion
2026-01-15

Countries

  • Austria
  • France
  • Germany
  • Switzerland

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 NCT07071740 on ClinicalTrials.gov