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New imaging method aims to personalize pelvic floor disorder treatments

NCT ID NCT04319653

Knowledge-focused 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
The trial has finished. Results may not be published yet.
Stopped early This study
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This status has not been confirmed recently, so it may be out of date.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 tested a new way to map the pelvic cavity in women using MRI and a special vaginal pressure probe. The goal was to better understand each woman's pelvic tissue characteristics so treatments like surgery or rehabilitation could be personalized. Only one participant was enrolled before the study was terminated, so the results are very limited.

What this could mean

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

What this could lead to
If successful, this could help doctors tailor surgeries or therapies for pelvic floor disorders based on each woman's unique tissue characteristics.
What could go wrong
The study was terminated early with only one participant, so the findings are very limited and may not apply to others.

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

1 person

The number who actually took part.

Started

Apr 2021

Finished

May 2021

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

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: All: * Understanding of the French language * Signature of informed consent * Insured social patient For pregnant women: * Primiparous women * with no severe maternal-fetal pathology * with no scheduled caesarean section at the time of the MRI For women with prolapse: \- Requires pelvic MRI Exclusion Criteria: * Minor * Person who does not have social security * Person with ongoing vaginal infection * Pregnant woman during the first or third trimester of pregnancy * Pregnant woman with broken water pocket * Bi-cicatricial uterus * IVF * Person wearing a pace maker or any intra-body metal implant (if "tube" MRI) * Claustrophobic person (if "tube" MRI)

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Conditions

The condition(s) this trial relates to.

Pelvic Floor Disorders pelvic organ prolapse

As listed by the trial registrant

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

Pelvic floor disorders

Contacts and locations

Locations

  • Hôpital Jeanne de Flandres, CHU

    Lille, France

More trials for these conditions

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