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Efficacy Study of Acupuncture to Relieve Symptoms of Chronic Prostatitis

A Double Blind, Sham Controlled Trial Evaluating the Efficacy of Acupuncture in Relieving Symptoms of Chronic Prostatitis/ Chronic Pelvic Pain Syndrome

Status
Completed
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00260637
Enrollment
86
Registered
2005-12-01
Start date
2004-02-29
Completion date
2005-08-31
Last updated
2006-10-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prostatitis

Keywords

Prostatitis

Brief summary

Limited evidence suggests that acupuncture may help relieve symptoms of chronic prostatitis/chronic pelvic pain syndrome. This study evaluated if acupuncture twice weekly for 10 weeks would help ameliorate symptoms of CP/CPPS.

Detailed description

Various studies have reported that this acupuncture able to relieve symptoms of chronic prostatitis (CP)/ chronic pelvic pain syndrome (CPPS). However, controversy exists on the efficacy of this technique due to poor experimental designs and lack of placebo controls in these experiment. This study is the first randomised controlled study which will evaluate if acupuncture for 10 weeks will help improve symptoms of CP/CPPS

Interventions

PROCEDUREAcupuncture

Sponsors

University of Washington
CollaboratorOTHER
Universiti Sains Malaysia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
MALE
Age
20 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Symptoms of discomfort or pain in the pelvic region for at least a three (3) months period within the last six (6) months. * Moderate overall score on the NIH-CPSI (overall score more than 15 out of a potential of 0-43 points) * Diagnosed as having CPPS Category III * Participant is willing to undergo 10 weeks of acupuncture treatment

Exclusion criteria

* History of prostate, bladder or urethral cancer. * Inflammatory bowel disease (such as Crohn's disease or ulcerative colitis, but not irritable bowel syndrome). * Undergone pelvic radiation or systemic chemotherapy, intravesical chemotherapy or intravesical BCG. * Treated for unilateral orchialgia without pelvic symptoms. * Active urethral stricture. * Undergone TURP, TUIP, TUIBN, TUMT, TUNA, balloon dilation of the prostate, open prostatectomy or any other prostate surgery or treatment such as cryotherapy or thermal therapy. * Neurological impairment or psychiatric disorder preventing his understanding of consent and his ability to comply with the protocol. * Liver disease. * Diagnosed as acute or chronic bacterial prostatitis. * History of urinary tract infection positive uropathogen for the past year. * Taking medications which could affect the lower urinary tract function * History of type 1 or 2 diabetes. * Treated/currently undergoing treatment with acupuncture for any other illness including prostatitis for the past 6 months. * Refusal to be needled or any form of bleeding disorder.

Design outcomes

Primary

MeasureTime frame
Six point drop in NIH-CPSI total Score

Secondary

MeasureTime frame
Individual domains of the NIH-CPSI
Patient reported Global Response Assessment
International Prostate Symptom Score
International Index of Erectile Function
Brief Pain Inventory- Short Form

Countries

Malaysia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 19, 2026