Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Cure My Disease

Don't miss your cure!

 Log in / Sign up

Surgery showdown: which cystocele repair holds up best?

NCT ID NCT02272361

Disease control Sponsor: University Hospital, Lille 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study compared two surgical techniques—laparoscopic sacropexy and vaginal mesh surgery—for repairing a cystocele (a type of pelvic organ prolapse). Researchers followed 220 women for four years to see which approach provided better symptom relief and fewer complications. The goal is to help doctors and patients choose the best option for long-term results.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
surgery (laparoscopic sacrocolpopexy or vaginal mesh surgery)
What this could lead to
If one technique proves better, it could guide surgeons toward the most effective and safer option for repairing a cystocele.
What could go wrong
This is a completed study comparing two established procedures, so no major breakthrough is expected. Results may show only small differences, and individual outcomes vary.

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.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

220 people

The number who actually took part.

Start date

Oct 2014

Finished

Jun 2018

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.

Ages

45 to 75 years

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: * All the patients included in the PROSPERE study will be included in the PROSPERE-4 study. The inclusion criterias for the PROSPERE study are: * Written informed consent * insured under the French social security system Exclusion Criteria: * Unwillingness or inability to comply with the requirements of this protocol, including the presence of any condition (physical, mental, or social) that is likely to affect the subject's ability to comply with the study protocol * Participation in another trial

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Cystocele are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

Conditions

The condition(s) this trial relates to.

Cystocele pelvic organ prolapse

As listed by the trial registrant

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

Cystocele

Contacts and locations

Locations

  • CH La Rochelle Service de Gynécologie Obstétrique

    La Rochelle, 17019, France

  • CHI Poissy-St-Germain / Service de gynécologie

    Poissy, 78303, France

  • CHRU de Lille - Service de Gynécologie médico chirurgicale

    Lille, 59037, France

  • CHU Estaing

    Clermont-Ferrand, 63003, France

  • CHU de Nîmes

    Nîmes, 30029, France

  • CHU de Poitiers

    Poitiers, 86000, France

  • GCS Flandre Maritime

    Grande-Synthe, 59760, France

  • Groupe Hospitalier Diaconesses Croix St-Simon

    Paris, 75571, France

  • Hôpital Antoine Béclère

    Clamart, 92140, France

  • Hôpital BICETRE / Service de Gynécologie Obstétrique

    Le Kremlin-Bicêtre, 94275, France

  • Hôpital de Hautepierre

    Strasbourg, 67000, France

  • Sébatien BLANC

    Annecy, 74374, France

More trials for these conditions

Other studies related to the condition(s) this trial covers.