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Robot-Assisted GYN surgery under the microscope: new study tracks Real-World outcomes

NCT ID NCT05867927

Knowledge-focused Sponsor: Intuitive Surgical Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Sep 11, 2026 · Updated 4 times

Summary

This study is observing how well robotic-assisted surgery works for women with gynecological conditions. It will follow 1,250 participants in Germany for up to 12 months after surgery to track complications, recovery, and patient-reported outcomes. The goal is to gather real-world evidence on the safety and effectiveness of the da Vinci Surgical System in routine care.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

About 1,250 people

The number the study aims to enrol. It can still change while the study runs.

Started

Oct 2023

Expected to finish

Mar 2028

An estimate. End dates often move.

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Patients with gynecological disease that may be treated by surgical intervention.

Ages

18 years and older

Sex

Female participants only

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Key Inclusion Criteria: * Woman with 18 years of age or older * Patient is willing to participate and to comply with the study procedures as demonstrated by signing the informed consent * Patient is a candidate for a gynecological procedure to be performed with the Intuitive Surgical System Key Exclusion Criteria: * Life expectancy of less than 1 year * Pregnancy, or positive pregnancy test for women prior to menopause or breastfeeding women * Current participation in a clinical study, if not pre-approved by Intuitive * Individuals who are unable to fully understand all aspects of the study that are relevant to the decision to participate (mentally or verbally), or who could be manipulated or unduly influenced as a result of a compromised position, expectation of benefits or fear of retaliation

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Conditions

The condition(s) this trial relates to.

female reproductive system disorder

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Gyn disorders

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    2 sites. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Agaplesion Markus Krankenhaus Frankfurt am Main

    ACTIVE_NOT_RECRUITING

    Frankfurt am Main, 60431, Germany

  • Albertinen Krankenhaus Hamburg

    ACTIVE_NOT_RECRUITING

    Hamburg, Free and Hanseatic City of Hamburg, 22457, Germany

  • Augusta-Kranken-Anstalt Bochum

    ACTIVE_NOT_RECRUITING

    Bochum, 44791, Germany

  • Charité - Universitätsmedizin Berlin - Klinik für Gynäkologie

    ACTIVE_NOT_RECRUITING

    Berlin, 13353, Germany

  • Helios Kliniken Schwerin

    ACTIVE_NOT_RECRUITING

    Schwerin, 19055, Germany

  • Klinikum Nürnberg Nord / Klinik für Frauenheilkunde

    ACTIVE_NOT_RECRUITING

    Nuremberg, 90419, Germany

  • Sana Kliniken Coburg

    ACTIVE_NOT_RECRUITING

    Coburg, 96450, Germany

  • St. Ansgar Krankenhaus Höxter

    ACTIVE_NOT_RECRUITING

    Höxter, 37671, Germany

  • St. Elisabeth-Krankenhaus Köln-Hohenlind

    TERMINATED

    Cologne, 50935, Germany

  • St. Josefs-Hospital Wiesbaden

    ACTIVE_NOT_RECRUITING

    Wiesbaden, Hesse, 65189, Germany

  • Universitätsklinikum Essen

    ACTIVE_NOT_RECRUITING

    Essen, 45147, Germany

  • Universitätsklinikum Freiburg - Klinik für Frauenheilkunde

    RECRUITING

    Freiburg im Breisgau, 79106, Germany

  • Universitätsklinikum Kiel

    ACTIVE_NOT_RECRUITING

    Kiel, 24105, Germany

  • Universitätsklinikum Tübingen - Frauenklinik

    ACTIVE_NOT_RECRUITING

    Tübingen, 72076, Germany

  • Universitätsmedizin Greifswald

    RECRUITING

    Greifswald, 17475, Germany