Acupuncture to reduce pain during prostate biopsy
Acupuncture for Analgesia in Transperineal Prostate Biopsy: A Randomized Controlled Trial
This study is testing if acupuncture can help reduce pain and improve the experience for men undergoing a prostate biopsy.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 110 (estimated) |
| Ages | 40 Years to 75 Years |
| Sex | Male |
| Sponsor | Medipol University Academic / other |
| Locations | 1 site (İstanbul) |
| Trial ID | NCT06987071 on ClinicalTrials.gov |
What this trial studies
This trial evaluates the effectiveness of acupuncture in alleviating pain and enhancing the patient experience during transperineal prostate biopsy. Participants will be randomly assigned to receive either acupuncture or a sham treatment, alongside standard local anesthesia. The primary focus is on measuring pain levels using the Visual Analog Scale (VAS), while secondary outcomes include anxiety levels, additional analgesic use, patient satisfaction, and any adverse events. The study aims to provide evidence on whether acupuncture can serve as a beneficial adjunct for pain management in this procedure.
Who should consider this trial
Good fit: Ideal candidates are men indicated for a transperineal prostate biopsy who can provide informed consent.
Not a fit: Patients with known allergies to acupuncture, those requiring sedation, or individuals with severe psychiatric disorders may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could offer a non-pharmacological option for pain relief during prostate biopsies, improving patient comfort and satisfaction.
How similar studies have performed: While acupuncture has shown promise in managing procedural pain in various settings, its specific application for transperineal prostate biopsy is relatively novel and underexplored.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Indicated for transperineal prostate biopsy (e.g., elevated PSA, abnormal digital rectal exam). * Willing and able to provide written informed consent. Exclusion Criteria: * Known allergy or contraindication to acupuncture (e.g., bleeding disorder, needle phobia). * Requirement for sedation or general anesthesia. * Previous experience with acupuncture treatment. * Severe psychiatric disorders or diagnosed anxiety disorder.
Where this trial is running
İstanbul
- İstanbul Başakşehir Çam ve sakura City Hospita — İstanbul, Turkey (Recruiting)
Study contacts
- Study coordinator: Ali İhsan Memmi
- Email: alimemmi@gmail.com
- Phone: 90 05379220997
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.