Clinical Efficacy of Multi-Focal Low-Intensity Extracorporeal Shockwave Therapy in the Treatment of Chronic Prostatitis/Chronic Pelvic Pain Syndrome: Prospective-Randomized, Double Blind, Placebo-Controlled Study

被引:1
|
作者
Kim, Kang Sup [1 ]
Choi, Yong Sun [2 ]
Bae, Woong Jin [3 ,4 ]
Cho, Hyuk Jin [3 ]
Ha, U-Syn [3 ]
Hong, Sung-Hoo [3 ]
Lee, Ji Youl [3 ]
Han, Chang Hee [1 ]
Kim, Sae Woong [3 ,4 ]
机构
[1] Catholic Univ Korea, Coll Med, Uijeongbu St Marys Hosp, Dept Urol, Uijongbu, South Korea
[2] Catholic Univ Korea, Coll Med, Eunpyeong St Marys Hosp, Dept Urol, Seoul, South Korea
[3] Catholic Univ Korea, Seoul St Marys Hosp, Coll Med, Dept Urol, 222 Banpo Daero, Seoul 06591, South Korea
[4] Catholic Univ Korea, Coll Med, Catholic Integrat Med Res Inst, Seoul, South Korea
来源
WORLD JOURNAL OF MENS HEALTH | 2022年 / 40卷 / 04期
关键词
Chronic pelvic pain syndrome; Low-intensity extracorporeal shock wave therapy; Multi-focal; WAVE-THERAPY; TRIPLE-THERAPY; MANAGEMENT; EFFICIENCY;
D O I
10.5534/wjmh.210078
中图分类号
R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
摘要
Purpose: To assess the safety and effect of the multifocal low-intensity extracorporeal shockwave therapy (MESWT) in the treatment of chronic prostatitis/chronic pelvic pain syndrome (CP/CPPS). Materials and Methods: We randomly separated 30 patients with CP/CPPS into a MESWT and placebo group of same number using prospective-randomized, double-blind design. The participants' National Institutes of Health Chronic Prostatitis Symptom Index (NIH-CPSI) total and subdomain scores, International Prostate Symptom Score (IPSS), International Index of Erectile Function-5 (IIEF-5), and visual analogue scale (VAS) were assessed and compared at baseline and at finishing immediately and 4 weeks after procedure and also were compared between MESWT and placebo group. Results: A total of 30 participants were randomized a MESWT or placebo group. Twenty of thirty participants completed this trial. NIH-CPSI total and subdomain scores, IPSS, IIEF-5, and VAS had significantly ameliorated compared with baseline in the MESWT group at 4 weeks assessment. Furthermore, comparison of the results from MESWT and placebo groups represented statistically significant differences in NIH-CPSI total and subdomain scores, IPSS, IIEF-5, and VAS. No side effects or events were occurred in both groups of the participants during study periods. Conclusions: MESWT can be an effective treatment modality in patients with CP/CPPS as it improves pain and QoL.
引用
收藏
页码:678 / 685
页数:8
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