Needles vs. leaks: acupuncture trial aims to dry up Post-Surgery accidents
NCT ID NCT07239518
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
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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
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About 144 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Dec 2025
An estimate. Start dates often move.
- Expected to finish
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Aug 2027
An estimate. End dates often move.
- Lead sponsor
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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
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50 to 85 years
- Sex
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Male participants only
- Healthy volunteers
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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 Hide 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.
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.
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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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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.
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- New PET tracer aims to light up hidden cancer targets
- Can daily adaptive radiotherapy spare healthy tissue in prostate cancer?
- Can a radioactive tracer and MRI reveal prostate Cancer's true extent?
- Five-Fraction radiation plus hormone therapy tested against High-Risk prostate cancer
- Can a 10-Hour eating window fight cancer fatigue?