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Needles vs. leaks: acupuncture trial aims to dry up Post-Surgery accidents

NCT ID NCT07239518

Symptom relief Sponsor: Bin Xu Source: ClinicalTrials.gov ↗

What the study statuses mean

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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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests whether starting acupuncture before the urinary catheter is removed can help men regain bladder control faster after prostate cancer surgery. 144 men will be randomly assigned to receive either real electroacupuncture or a sham (fake) version. The main goal is to measure urine leakage in the first week after catheter removal, with follow-ups over 24 weeks.

What this could mean

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

Active substance
electroacupuncture
What this could lead to
If it works, this could offer a simple, non-drug way to help men regain bladder control sooner after prostate cancer surgery.
What could go wrong
This is an early-stage study with a small number of participants. The sham acupuncture group may also show improvement, and the real acupuncture might not provide additional benefit. Results may not apply to all patients.

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 144 people

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

Expected to start

Dec 2025

An estimate. Start dates often move.

Expected to finish

Aug 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.

Ages

50 to 85 years

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: 1. Patients who have undergone radical prostatectomy with a confirmed pathological diagnosis of prostate cancer. 2. One week post-radical prostatectomy (RP). 3. Karnofsky Performance Score (KPS) ≥ 60 or ECOG Performance Status 0-1. 4. Age between 50 and 85 years. 5. Signed informed consent. Exclusion Criteria: 1. Pathological results show positive surgical margins. 2. Previous treatment for post-operative urinary incontinence, such as cystostomy, urethral sphincter reconstruction, or urethral suspension. 3. Currently or within the last 6 months receiving treatment with principles similar to acupuncture (e.g., electroacupuncture, moxibustion, warm moxibustion). 4. Active urinary system infection (excluding asymptomatic lower urinary tract infection). 5. Known severe heart diseases, such as severe arrhythmia, severe heart failure, acute myocarditis, constrictive pericarditis, pericardial tamponade, severe valvular disease, or heart failure. 6. Known liver damage or potential severe liver disease (ALT or AST \> 10 times the normal limit). 7. Known severe renal impairment (eGFR \< 25mL/min/1.73m2), planned or ongoing dialysis, or acute contrast-induced nephropathy at screening. 8. Known dysfunction of other vital organs or severe primary diseases, such as hematopoietic system diseases. 9. Known coagulation dysfunction (with typical clinical diagnosis or clear laboratory test results). 10. Patients with mental illness or cognitive impairment; patients with severe depression, alcohol dependence, or a history of drug abuse. 11. Urinary incontinence known to be due to other reasons. 12. According to the investigator's judgment, the patient is not suitable for this study or has a high probability of dropout (e.g., frequent changes in work environment that make follow-up difficult). 13. Life expectancy ≤ 6 months, as judged by the investigator. 14. Currently participating in other clinical trials.

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Conditions

The condition(s) this trial relates to.

prostate cancer Urinary Incontinence

As listed by the trial registrant

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

How to take part

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  1. The official record

    The full official record for this study. This one lists no contact details, but it is the first place any would appear.

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  2. A doctor treating you

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More trials for these conditions

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