Benign Prostatic Hyperplasia Clinical Trial
Official title:
A Pilot Study on Effectiveness and Safety of Moxibustion for Benign Prostate Hyperplasia With Lower Urinary Tract Syndrome
This study aims to explore the feasibility of moxibustion as a supplementary intervention and to assess the sample size for verifying the effectiveness and safety of integrative treatment involving moxibustion compared with conventional treatment for patients with benign prostate hyperplasia (BPH) accompanying moderate to severe lower urinary tract symptoms (LUTS).
Patients who diagnosed as BPH with moderate to severe LUTS aged 20 to 80 years old will be
divided into two groups, one is moxibustion plus conventional therapy group and the other is
conventional therapy group.
Patients who belong to moxibustion plus conventional therapy group will be treated
moxibustion for eight times by a Korean Medicine doctor with conventional therapy by a
urologist.
Patients who belong to conventional therapy group will be treated with conventional therapy
only, and they can receive moxibustion therapy after the clinical trial is finished.
IPSS, post void residual volume (PVR) and peak urine flow (Qmax) will be checked to evaluate
the effectiveness and safety.
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