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New sexuality questionnaires tested for women with bladder or pelvic issues

NCT ID NCT01632839

Knowledge-focused Sponsor: Centre Hospitalier Universitaire de Nīmes Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026

Summary

This study tested two French questionnaires about sexuality in 298 women who had surgery for urinary incontinence, pelvic organ prolapse, or fecal incontinence. The goal was to see if these questionnaires accurately measure sexual function compared to an existing tool. No treatment or medication was given—this was purely a validation study.

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

298 people

The number who actually took part.

Started

Jan 2013

Finished

Apr 2017

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

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 undergoing vaginal, abdominal or urinary incontinence surgery.

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.

Inclusion Criteria: * Patient is not pregnant * Patient can read and understand French * The patient must have given her informed and signed consent * The patient must be insured or beneficiary of a health insurance plan * The patient has genital prolapse and/or urinary incontinence and/or anal incontinence, and have undergone surgery Exclusion Criteria: * The patient is under judicial protection * The patient does not understand french * Patient has vulvodynia * Patient has painful bladder syndrome * The patient has had chronic pelvic pain for longer than 6 months

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Conditions

The condition(s) this trial relates to.

Fecal Incontinence pelvic organ prolapse Sexuality Urinary Incontinence

As listed by the trial registrant

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

Fecal incontinence Pelvic organ prolapse Sexuality Urinary incontinence

Contacts and locations

Locations

  • APHP - Centre Hospitalier Universitaire de Bicêtre

    Le Kremlin-Bicêtre, 94275, France

  • APHP - Hôpital Antoine Beclere

    Clamart, 92141, France

  • APHP - Hôpital Bichat - Claude Bernard

    Paris, 75877, France

  • CH de Poissy - Saint-Germain-en-Laye

    Saint-Germain-en-Laye, 78100, France

  • CH de la Rochelle

    La Rochelle, 17019, France

  • CH de la Région d'Annecy

    Pringy, 74374, France

  • CHRU de Lille - Hôpital Jeanne de Flandre

    Lille, 59037, France

  • CHRU de Strasbourg - Hôpital de Hautepierre

    Strasbourg, 67098, France

  • CHU de Clermont Ferrand - Hôpital Estaing

    Clermont-Ferrand, 63003, France

  • CHU de Nîmes - Hôpital Universitaire Carémeau

    Nîmes, 30029, France

  • CHU de Poitiers

    Poitiers, 86021, France

  • G.C.S. Flandre Maritime - site Polyclinique de Grande-Synthe

    Grande-Synthe, 59760, France

  • Groupe Hospitalier Dioconesses - Site Reuilly

    Paris, 75012, France

  • Hôpital Foch

    Suresnes, 92151, France

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