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Effect of fire needle therapy on mild-moderate benign prostatic hyperplasia: Protocol for a randomized controlled pilot trial

Effect of fire needle therapy on mild-moderate benign prostatic hyperplasia: Protocol for a randomized controlled pilot trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2000003205
Enrollment
Unknown
Registered
2020-04-12
Start date
2020-07-01
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

mild-moderate benign prostatic hyperplasia

Interventions

Sponsors

Beijing Hospital of Traditional Chinese Medicine, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged 40–80 years old; 2. diagnosed with BPH for more than 3 months; 3. syndrome differentiation in traditional Chinese medicine conforms to kidney yang deficiency; 4. abstain from medication for BPH for more than 6 months before the start of treatment; 5. IPSS score < 19 (mild-moderate BPH); 6. Qmax<15mL/s or average flow rate (Qave)<10ml/s; 7. with stable life signs; 8. voluntary participation in the study and sign informed consent prior to treatment.

Exclusion criteria

Exclusion criteria: 1. oliguria and anuria caused by bladder or prostate malignancy, urolithiasis, acute/chronic renal failure; 2. urinary dysfunction caused by neurogenic bladder, bladder neck fibrosis, and urethral stricture; 3. gonorrhea and urinary tract infection; 4. failure of invasive therapy for BPH; 5. local organs, muscles and nerves injured by pelvic operation or trauma; 6. abdominal aneurysms, hepatosplenomegaly, and serious cerebrovascular, cardiovascular, respiratory, digestive, hematological, or psychiatric diseases; 7. blood coagulation disorders or requiring administration of anticoagulant medication, such as Warfarin and Dabigatran; 8. cognitive dysfunction, psychosis, unable to cooperate with the examination and treatment.

Design outcomes

Primary

MeasureTime frame
International prostate symptom score;

Secondary

MeasureTime frame
Mean number of nightly urinations;Average flow rate (Qave);Prostate volume;Maximum urinary flow rate (Qmax);

Countries

China

Contacts

Public ContactTao Zhang

Beijing Hospital of Traditional Chinese Medicine, Capital Medical University, Beijing, China

tony_ever@hotmail.com+86 13581901177

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026