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

Gå till den engelska sidan

Routine pee test before bladder surgery may be unnecessary, major study suggests.

NCT ID NCT07463963

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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 Results may not be published yet.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
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This status has not been confirmed recently, so it may be out of date.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 Sep 04, 2026 · Updated 4 times

Summary

This study will include 2,600 adults scheduled for bladder tumor surgery. Half will get a standard urine culture before surgery; the other half will not. The goal is to see if skipping the test leads to more fevers or infections in the month after surgery. If it's safe, it could save time and resources.

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 simplify pre-surgery preparation for bladder tumor patients, reducing delays and healthcare costs without increasing infection risk.
What could go wrong
This is an early-stage trial (not yet recruiting) comparing two standard approaches, so results may not change practice if infection rates rise without urine cultures.

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 2,600 people

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

Started

Jun 2026

Expected to finish

Aug 2030

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.

Ages

18 years and older

Sex

Anyone

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 aged 18 or over * Scheduled for TURB surgery for a suspected or confirmed diagnosis of bladder tumor * Affiliated person or beneficiary of a social security scheme * Written informed consent obtained from the participant Exclusion Criteria: * Patient with active UTI * Planned combined surgery * Patient previously included in this research protocol * People benefiting from enhanced protection, namely minors, people deprived of their liberty by judicial or administrative decision, people staying in a health or social institution, adults under legal protection * Pregnant or breastfeeding women, women of childbearing age who do not have effective contraception (Combined (estrogen and progestogen containing) hormonal contraception associated with inhibition of ovulation : oral, intravaginal, transdermal; Progestogen-only hormonal contraception associated with inhibition of ovulation : oral, injectable, implantable; Intrauterine device; Intrauterine hormone-releasing system; Bilateral tubal occlusion) or permanent sterilization methods ( hysterectomy, bilateral salpingectomy, bilateral oophorectomy).

Get updates

Get notified about this study

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

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

How to take part

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

  1. The places running it

    15 sites. The list below names each one and where it is.

  2. 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 ↗

  3. 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.

Contacts and locations

Locations

  • AP-HP - Hôpital Universitaire Pitié-Salpêtrière

    NOT_YET_RECRUITING

    Paris, 75013, France

  • Assistance Publique - Hôpitaux de Marseille - Hôpital Nord

    NOT_YET_RECRUITING

    Marseille, 13354, France

  • CHU Poitiers - Service de chirurgie urologique

    RECRUITING

    Poitiers, 86000, France

  • Centre Hospitalier Intercommunal de Mont de Marsan et du Pays des Sources

    RECRUITING

    Mont-de-Marsan, 40024, France

  • Centre Hospitalier Régional et Universitaire de Nancy - Hôpitaux de Brabois

    NOT_YET_RECRUITING

    Vandœuvre-lès-Nancy, 54500, France

  • Centre Hospitalier Régional et Universitaire de Tours - Bretonneau

    NOT_YET_RECRUITING

    Tours, 37044, France

  • Centre Hospitalier Universitaire d'Angers

    NOT_YET_RECRUITING

    Angers, 49100, France

  • Centre Hospitalier Universitaire de Grenoble Alpes

    NOT_YET_RECRUITING

    Grenoble, 38043, France

  • Centre Hospitalier Universitaire de Lille

    NOT_YET_RECRUITING

    Lille, 59037, France

  • Centre Hospitalier Universitaire de Nantes - Hotel Dieu

    NOT_YET_RECRUITING

    Nantes, 44093, France

  • Centre Hospitalier de Chartres - Hôpital Louis Pasteur

    NOT_YET_RECRUITING

    Le Coudray, 28630, France

  • Centre hospitalier universitaire de Bordeaux

    NOT_YET_RECRUITING

    Talence, 33404, France

  • Clinique la Croix du Sud

    NOT_YET_RECRUITING

    Quint-Fonsegrives, 31130, France

  • Hospices Civils de Lyon

    RECRUITING

    Lyon, 69229, France

  • Hôpital Bichat Claude Bernard-APHP

    NOT_YET_RECRUITING

    Paris, 75018, France

More trials for these conditions

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