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Title

Efficacy and Safety of Guihuang Formula in Treating Type III Prostatitis Patients with Dampness-Heat and Blood Stasis Syndrome: A Randomized Controlled Trial.

Authors

Liu SJ, Deng YJ, Zeng Y, Zhao M, Guo J, Gao QH. 

Journal

Chin J Integr Med.

Year

2022

Vol (Issue)

Online ahead of print.

Page

doi

10.1007/s11655-022-3467-1.

PMID

35419726

Url

http://www.ncbi.nlm.nih.gov/pubmed/35419726

MeSH

Chronic Disease
Hot Temperature
Humans
Lecithins
Male
Pain
*Prostatitis/drug therapy
Quality of Life
Tamsulosin
Chinese medicine
Guihuang Formula
dampness-heat and blood stasis syndrome
randomized controlled trial
type III prostatitis

Keywords

Chinese medicine; Guihuang Formula; dampness-heat and blood stasis syndrome; randomized controlled trial; type III prostatitis

한글 키워드

중약; 귀황탕; 습열혈어증; 무작위배정 비교임상연구; 만성 전립선염/만성 골반통 증후군

KMCRIC
Summary & Commentary

KMCRIC 비평 보기 +

Korean Study

Abstract

Objective: To observe the efficacy and safety of Guihuang Formula (GHF) in treating patients with type III prostatitis and Chinese medicine syndrome of dampness-heat and blood stasis.

Methods: Sixty-six patients diagnosed with type III prostatitis with dampness-heat and blood stasis syndrome were randomly divided into the treatment group (GHF) and the control group (tamsulosin) using a random number table, with 33 cases each group. The treatment group received GHF twice a day, and the control group received tamsulosin 0.2 mg once daily before bedtime. Patients in both groups received treatment for 6 weeks and was followed up for 2 weeks. The outcomes included the National Institute of Health Chronic Prostatitis Symptom Index (NIH-CPSI) score, Chinese Medicine Symptoms Score (CMSS), expressed prostatic secretions (EPS) and adverse events (AEs).

Results: After treatment, the NIH-CPSI total score and domain scores of pain discomfort, urination and quality of life decreased significantly from the baseline in both groups (P<0.05). The CMSS score decreased in both groups (P<0.05). The WBC count decreased and lecithin body count increased in both groups (P<0.05). GHF showed a more obvious advantage in reducing the pain discomfort and quality of life domain scores of NIH-CPSI, reducing the CMSS score, increasing the improvement rate of the WBC and lecithin body counts, compared with the control group (P<0.05). There were no significant differences in decreasing urination domain score of NIH-CPSI between two groups (P>0.05). In addition, no serious AEs were observed.

Conclusion: GHF is effective in treating type III prostatitis patients with dampness-heat and blood stasis syndrome without serious AEs. (Registration No. ChiCTR1900026966).

© 2022. The Chinese Journal of Integrated Traditional and Western Medicine Press and Springer-Verlag GmbH Germany, part of Springer Nature.

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