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Scientists to peek inside bladder during catheterization with upright MRI

NCT ID NCT07384559

Knowledge-focused Sponsor: Coloplast A/S 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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This exploratory study will use an upright MRI scanner to take 3D images of the bladder in 20 people—some with spinal cord injury who use catheters, and some healthy volunteers. The goal is to understand how the bladder and surrounding structures change shape during catheter use and normal voiding. The study does not test any treatment, but aims to gather knowledge that could improve future 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.

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

About 20 people

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

Expected to start

Mar 2026

An estimate. Start dates often move.

Expected to finish

Jul 2026

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.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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: 1. Has given written informed consent 2. Is at least 18 years old 3. Has full legal capacity 4. Is able (assessed by investigator) and willing to adhere to study procedures during study duration 5. Is able (assessed by investigator) to remain seated in the MRI scanner for minimum 20 minutes\* 6. Known with SCI for a minimum of 1 year\* 7. Has used IC as primary bladder emptying method for at least 3 months\* \* Only for SCI subjects Exclusion Criteria: 1. Is participating in any other clinical investigation during this investigation 2. Has previously completed this investigation 3. Has any known allergic or hypersensitive reactions to any device or its ingredients used in the investigation 4. Is pregnant 5. Has had surgical procedures performed in the lower urinary tract. 6. Has active/recurrent bladder cancer 7. Has experienced autonomic dysreflexia within the last 2 years 8. Has any MRI-scanning contraindications, according to MR check list provided by the site (e.g. active implants like pacemaker, cochlear implant, event recorder, implanted insulin pump) 9. Has symptoms of UTI at times of inclusion, as judged by the investigator. 10. Has a body weight that exceeds the maximum of 150kg max

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Conditions

The condition(s) this trial relates to.

spinal cord injury Urinary Retention

As listed by the trial registrant

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

Retention, urinary

How to take part

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

  1. 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 ↗

  2. 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.

More trials for these conditions

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