Actively Recruiting

Phase Not Applicable
Age: 40Years - 80Years
MALE
NCT05585450

Effect of Electroacupuncture on Benign Prostatic Hyperplasia

Led by Guang'anmen Hospital of China Academy of Chinese Medical Sciences · Updated on 2024-07-18

306

Participants Needed

1

Research Sites

146 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The study aims to assess the efficacy and safety of electroacupuncture among men with benign prostatic hyperplasia (BPH), compared with sham electroacupuncture.

CONDITIONS

Official Title

Effect of Electroacupuncture on Benign Prostatic Hyperplasia

Who Can Participate

Age: 40Years - 80Years
MALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of benign prostatic hyperplasia according to European Association of Urology guidelines
  • Male participants aged between 40 and 80 years
  • Experiencing lower urinary tract symptoms for at least three months
  • International Prostate Symptom Score (IPSS) total score of 8 or higher
  • Prostate volume of 20 mL or more
  • Urinary peak flow rate (Qmax) of 15 mL/s or less
  • Willingness to participate voluntarily and signed written informed consent
Not Eligible

You will not qualify if you...

  • Post-void residual urine volume of 150 mL or more
  • Acute urinary retention or catheterization for outflow obstruction within the past 3 months (except post-surgical disposable catheterization)
  • Prostate cancer or prostate-specific antigen (PSA) level of 4.0 ng/mL or higher
  • Neurogenic lower urinary tract dysfunction, prostatitis, uncontrolled symptomatic urinary tract infections, urethral strictures, bladder diverticula, bladder stones, bladder cancer, or history of genitourinary surgery
  • Previous acupuncture treatment for BPH in the last month or use of alpha-blockers, 5-alpha-reductase inhibitors, muscarinic receptor antagonists, or other specific medications in the past two weeks unless stable 5-alpha-reductase inhibitor use for over three months
  • Severe lung, heart, liver, kidney, metabolic, or mental illness; coagulation dysfunction; or obvious cognitive dysfunction
  • Installed cardiac pacemaker, allergy to metal, severe fear of acupuncture, or inability to tolerate electroacupuncture stimulation

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Guang'anmen Hospital, China Academy of Chinese Medical Sciences

Beijing, Beijing Municipality, China, 100053

Actively Recruiting

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Research Team

Z

Zhishun Liu

CONTACT

L

Lili Zhu

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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