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Versius Gynecology Study

NCT07289295 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 45

Last updated 2025-12-17

No results posted yet for this study

Summary

The objective of this clinical trial is to expand the clinical evaluation of the safety and efficacy of Versius in gynaecology procedures of total robotic assisted hysterectomy and/or salpingo-oophorectomy

Conditions

  • Robotic Assisted Hysterectomy and/or Salpingo-oophorectomy

Interventions

DEVICE

Versius Surgical System

Modular robotic system intended to assist in the accurate control of its surgical endoscopic instruments across a range of surgical procedures

Sponsors & Collaborators

  • Uniwersyteckie Centrum Kliniczne im. prof. K. Gibińskego Śląskiego Uniwersytetu Medycznego w Katowicach

    collaborator UNKNOWN

  • CMR Surgical Ltd

    lead INDUSTRY

Principal Investigators

  • Krzysztof Nowosielski, MD · Uniwersyteckie Centrum Kliniczne im. prof. K. Gibińskego Śląskiego Uniwersytetu Medycznego w Katowicach

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
22 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-07-25
Primary Completion
2025-12-31
Completion
2026-01-31

Countries

  • Poland

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 NCT07289295 on ClinicalTrials.gov