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Could removing catheters hours after surgery speed recovery?

NCT ID NCT07768878

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Aug 17, 2026 · Last updated Aug 18, 2026 · Updated 1 time

Summary

This trial tests whether removing the urinary catheter and vaginal pack about 6 hours after pelvic organ prolapse surgery—instead of the usual 1-2 days—helps women recover faster. Researchers will compare time to first urination, walking ability, hospital stay length, and patient satisfaction. The study involves about 97 women undergoing vaginal prolapse repair at a single hospital in Singapore.

What this could mean

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

Active substance
Early removal of the indwelling urinary catheter and vaginal pack, about 6 hours after surgery, instead of waiting 1-2 days.
What this could lead to
If successful, this could shorten hospital stays, speed up recovery, and reduce healthcare costs for women undergoing prolapse surgery.
What could go wrong
This is a small, single-center trial, and early removal may increase the risk of urinary retention or the need for catheter reinsertion in some women.

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

97 people

The number who actually took part.

Started

Apr 2024

Finished

Oct 2025

Lead sponsor

A government agency

The lead sponsor is a government body.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

21 to 99 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: * type of operation: vaginal route surgery for the correction of pelvic organ prolapse (vaginal hysterectomy and/or pelvic floor repair and/or vault suspension and/or colpocleisis and/or manchester) * ADL (activities of daily living) independent * Community ambulant * good discharge support * age 21 years old and above (adult) * all ASA scores * all BMI * patients in KK Women's and Children's Hospital (single-centre) Exclusion Criteria: * operations that are traditionally done as same day operation (MUS alone) * non-vaginal route, including laparoscopy/open/ mix of both * recurrent/chronic urinary retention * pre-op UDS (urodynamic studies): high RU (residual urine) \>150ml * current urinary tract infection at time of op * bilateral hydronephrosis * neurological disorders affecting incontinence / neurological bladder

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Conditions

The condition(s) this trial relates to.

pelvic organ prolapse Postoperative Complications

As listed by the trial registrant

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

Contacts and locations

Locations

  • KK Women's and Children's Hospital

    Singapore, Singapore, 229899, Singapore

More trials for these conditions

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