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Robotic Sacrocolpopexy and Sacrocervicopexy - an Observational Study to Confirm the Peri- and Postoperative Safety and Clinical Performance

NCT07031050 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 35

Last updated 2026-04-13

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 robotic-assisted sacrocolpopexy or sacrocervicopexy.

Conditions

  • Sacrocolpopexy

Interventions

DEVICE

sacrocolpopexy or sacrocervicopexy

Robotic-assisted sacrocolpopexy or sacrocervicopexy 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
2025-05-19
Primary Completion
2026-01-06
Completion
2026-01-06

Countries

  • 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 NCT07031050 on ClinicalTrials.gov