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Shock therapy for needle jitters: AcuTENS tested in prostate biopsy

NCT ID NCT07292337

Symptom relief Sponsor: University of Malaya Source: ClinicalTrials.gov ↗

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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 a gentle electrical current applied to specific points on the skin (AcuTENS) can reduce pain and anxiety during a prostate biopsy. About 53 men having their first biopsy will receive either active AcuTENS or a placebo device, on top of standard numbing medication. The goal is to see if this simple, low-risk technique can make the procedure more comfortable.

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

53 people

The number who actually took part.

Started

Dec 2024

Expected to finish

Nov 2026

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

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. Patient consented for first time TRUS prostate biopsy. 2. Patient aged 18 years and above. Exclusion Criteria: 1. Patient with previous experience of TRUS biopsy 2. Patient with pacemakers or automatic cardiac defibrillator implant or implant in the upper limb 3. Patient with cutaneous skin breaks on application sites (e.g wound, burn scar) 4. Patient diagnosed to have epilepsy or impaired mental state or anxiety disorder 5. Patient with known allergy to acupuncture patch or lidocaine spray

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Conditions

The condition(s) this trial relates to.

agnosia prostate cancer

As listed by the trial registrant

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

Procedural pain relief Prostate cancer Transcutaneous electrical nerve stimulation Transrectal ultrasound-guided prostate biopsy

Contacts and locations

Locations

  • University of Malaya

    Kuala Lumpur, Kuala Lumpur, 50603, Malaysia

More trials for these conditions

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