Nam Eun-Young, Park Ju-Yeon, Jo Junyoung, Jung Seung-Hyun, Lim Chi-Yeon, Kim Dong-Il
Department of Obstetrics & Gynecology, College of Korean Medicine, Gachon University Dongincheon Gil Korean Medicine Hospital, 21 Keunumul-ro, Jung-gu, Incheon, 22318, Republic of Korea.
Research institute of Korean Medicine, College of Korean Medicine, Dongguk University, 32 Dongguk-ro, Ilsandong-gu, Goyang-si, Gyeonggi-do, 10326, Republic of Korea.
Trials. 2018 Sep 15;19(1):493. doi: 10.1186/s13063-018-2715-3.
Electroacupuncture has been used for treatment in patients with overactive bladder. This study was conducted to evaluate the efficacy and safety of electroacupuncture for treating overactive bladder of postmenopausal women.
METHODS/DESIGN: This is a multicenter, randomized controlled, parallel clinical trial. Two hundred ninety participants with overactive bladder syndrome will be recruited from Dongguk University Bundang Oriental Hospital and Cheonan Korean Medicine Hospital of Daejeon University and randomly allocated into one of two groups in a 1:1 ratio. One group will receive electroacupuncture (EA) and the other acupuncture (AC). The allocation will be concealed from both participants and assessors. The study period will be about 10 weeks, including 6 weeks of electroacupuncture or acupuncture treatment and a four week follow-up period. Both EA group and AT group will undergo acupuncture at 7 fixed points, and the EA group will undergo electronic stimulation at 6 points. The primary outcome will be the average number of micturitions per 24 h based on a 3-day bladder diary. The secondary outcome will comprise the 3-day bladder diary, the overactive bladder symptom score and the results of the King's health questionnaire.
The results of this trial will provide information regarding the efficacy and safety of electroacupuncture for treating overactive bladder in postmenopausal women.
ClinicalTrials.gov, NCT03260907 . Registered on 24 August 2017.
电针已用于膀胱过度活动症患者的治疗。本研究旨在评估电针治疗绝经后女性膀胱过度活动症的疗效和安全性。
方法/设计:这是一项多中心、随机对照、平行临床试验。将从东国大学盆唐韩医医院和大田大学忠南韩医医院招募290名膀胱过度活动症患者,并以1:1的比例随机分配到两组中的一组。一组将接受电针治疗(EA),另一组接受针刺治疗(AC)。参与者和评估者均对分配情况不知情。研究期约为10周,包括6周的电针或针刺治疗以及4周的随访期。电针组和针刺组均将在7个固定穴位进行针刺,电针组将在6个穴位进行电刺激。主要结局将是基于3天膀胱日记得出的每24小时平均排尿次数。次要结局将包括3天膀胱日记、膀胱过度活动症症状评分和国王健康问卷结果。
本试验结果将提供有关电针治疗绝经后女性膀胱过度活动症的疗效和安全性的信息。
ClinicalTrials.gov,NCT03260907。于2017年8月24日注册。