Can acupuncture needles replace pain pills during prostate biopsy?
NCT ID NCT07069049
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether adding electroacupuncture to standard local anesthesia can lower pain and anxiety in men undergoing a prostate biopsy. 190 participants will receive either real or sham electroacupuncture during the procedure. The goal is to see if this ancient technique can make a common cancer test more comfortable.
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, drug-free way to reduce pain and anxiety during prostate biopsies.
- What could go wrong
- This is an early-stage study with only 190 participants, and the sham control may show similar effects. 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 190 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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Sep 2026
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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18 to 80 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: \- (1) To voluntarily participate in the study, I or his legal representative signed a written informed consent. (2) 18-80 years old (including 18 and 80 years old), male. (3) in accordance with the indication of prostate biopsy. Exclusion Criteria: * (1) in the stage of acute genitourinary infection or fever. (2) patients with chronic pain (such as bone metastasis of prostate cancer, knee osteoarthritis, scapulohumeral periarthritis, etc.) or acute pain (tonsillitis, acute lumbar sprain, etc.) before surgery. (3) Continuous use of anti-anxiety or analgesic drugs (use of anti-anxiety drugs or analgesics for more than 1 week in the past 3 months). (4) in the decompensated stage of cardiac insufficiency; A disease with a tendency to bleed heavily. (5) severe immunosuppression. (6) hypertension, diabetes and other complications were poorly controlled or unstable. (7) complicated with severe internal or external hemorrhoids, perianal or rectal lesions, and anal stenosis. (8) perineal skin ulceration, infection, and abnormal skin sensation. (9) patients with serious psychological diseases or uncooperative puncture. (10) allergy to narcotic drugs and fear of acupuncture operators. (11) Participants who participated in other clinical trials within 3 months before enrollment. (12) other conditions considered by the investigator to be inappropriate to participate in the trial.
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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
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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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