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Robotic Minimally Invasive Inguinal Hernia Repair With Dexter

NCT05873582 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 50

Last updated 2024-01-05

No results posted yet for this study

Summary

This study aims to confirm the perioperative and early postoperative safety and clinical performance (efficacy) of the Dexter Robotic System, in patients undergoing primary transperitoneal unilateral or bilateral inguinal hernia repair.

Conditions

  • Inguinal Hernia Repair

Interventions

DEVICE

Robotic-assisted inguinal hernia repair

Primary transperitoneal unilateral or bilateral inguinal hernia repair with the Dexter robotic system

Sponsors & Collaborators

  • Confinis

    collaborator INDUSTRY

  • Distalmotion SA

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-06-02
Primary Completion
2023-10-23
Completion
2023-10-23

Countries

  • 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 NCT05873582 on ClinicalTrials.gov