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European registry to reveal best surgery for leaky bladder in men

NCT ID NCT02757274

Knowledge-focused Sponsor: European Association of Urology Research Foundation 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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 study follows over 1000 men across Europe who had surgery for stress urinary incontinence (leaking urine with coughing, sneezing, or activity). The two surgeries being tracked are the artificial urinary sphincter and the male sling. Researchers will collect data for up to 10 years to see how well each surgery works and how long the benefits last.

What this could mean

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

Active substance
artificial urinary sphincter or male sling
What this could lead to
If successful, this registry could help doctors understand which surgery works best and for whom, improving treatment decisions for male stress incontinence.
What could go wrong
This is an observational registry, not a controlled trial, so it cannot prove one surgery is better. Results depend on how consistently centers report data.

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

1,054 people

The number who actually took part.

Started

Feb 2017

Expected to finish

Jul 2027

An estimate. End dates often move.

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

Male patients undergoing surgery for treatment of stress urinary incontinence by AUS or male sling

Ages

Children (under 18), adults (18 to 64) and older adults (65 and over)

Sex

Male 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: * Male patient undergoing surgery for stress incontinence by AUS or male sling. * Participant is willing and able to complete the questionnaires and give informed consent for participation in the study. Exclusion Criteria: * Participating center is unable to contribute consecutive patients.

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Conditions

The condition(s) this trial relates to.

female stress incontinence Urinary Incontinence, Stress

As listed by the trial registrant

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

Urinary incontinence,stress

Contacts and locations

Locations

  • AZ Groeninge

    Kortrijk, 8500, Belgium

  • Addenbrookes Hospital

    Cambridge, CB2 0QQ, United Kingdom

  • Fondazione Policlinico Universitario Agostino Gemelli IRCCS

    Rome, Italy

  • Germans Trias i Pujol Universitary Hospital

    Barcelona, 08916, Spain

  • Guy's Hospital

    London, SE1 9RT, United Kingdom

  • Helsinki University Hospital

    Helsinki, 00029 HUS, Finland

  • Hospital General Universitario Gregorio Marañón

    Madrid, 08916, Spain

  • Hospital Puerta de Hierro Majadahonda

    Madrid, 28222, Spain

  • Hospital Universitario 12 de Octubre

    Madrid, 28041, Spain

  • Hospital Universitario La Paz

    Madrid, 3008, Spain

  • Hospital Universitario Morales Meseguer

    Murcia, 3008, Spain

  • Hospital Universitario Ramón y Cajal

    Madrid, Spain

  • Hospital Universitario Virgen de las Nieves

    Granada, 18003, Spain

  • Hospital Universitario de Canarias

    San Cristóbal de La Laguna, 38320, Spain

  • Jessa Ziekenhuis campus Salvator

    Hasselt, 3500, Belgium

  • Oslo University Hospital, Rikshospitalet

    Oslo, 0372, Norway

  • Royal National Orthopaedic Hospital

    Stanmore, HA7 4LP, United Kingdom

  • Thomayer Hospital

    Prague, 140 59, Czechia

  • UMC Radboud

    Nijmegen, 6525 GA, Netherlands

  • UZ Leuven

    Leuven, 3000, Belgium

  • Universitetssykehuset Nord-Norge

    Narvik, 8516, Norway

  • University Hospital Antwerpen

    Antwerp, 2650, Belgium

  • University Hospital Gent

    Ghent, 9000, Belgium

  • University Hospital La Fe

    Valencia, 46026, Spain

  • University Medical Center Hamburg Eppendorf

    Hamburg, 20246, Germany

  • University Medical Center Utrecht

    Utrecht, 3584 CX, Netherlands

  • University Münster

    Münster, 48149, Germany

  • Universitätsmedizin Mainz

    Mainz, 55131, Germany

More trials for these conditions

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