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首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >Effectiveness and Safety of Electroacupuncture on Poststroke Urinary Incontinence: Study Protocol of a Pilot Multicentered, Randomized, Parallel, Sham-Controlled Trial
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Effectiveness and Safety of Electroacupuncture on Poststroke Urinary Incontinence: Study Protocol of a Pilot Multicentered, Randomized, Parallel, Sham-Controlled Trial

机译:电针对预测尿失禁的有效性和安全性:试点多元化,随机,平行,假手术试验的研究方案

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摘要

This pilot multicentered, randomized, parallel, sham-controlled trial is intended to evaluate the effectiveness and safety of electroacupuncture therapy for poststroke patients with urinary incontinence. Forty stroke survivors aged >19 years will be recruited in 2 hospitals in the Republic of Korea. Patients who experienced stroke within 2 years and satisfy criteria of urinary frequencies >2 with either 3 to 4 points on the Patient Perception of Intensity of Urgency Scale or 13 points or more on the Korean version of the International Prostate Symptom Scale (K-IPSS) will be identified, along with other eligibility criteria. Patients will be randomly allocated to either a treatment or control group to receive 10 sessions of electroacupuncture or sham therapies, respectively. Patients and outcome assessors will be blinded. The primary outcome is the change of Total Urgency and Frequency Score between the baseline and the trial endpoint. The K-IPSS, the International Consultation on Incontinence Questionnaire for Urinary Incontinence Short Form, and the Lower Urinary Tract Symptoms Outcome Score will be evaluated for effectiveness assessment. Adverse events will be reported after every session. The Bunding Index will also be calculated. Data will be statistically analyzed with 0.05 significance levels by 2-sided testing.
机译:该试点多中心,随机,并行,假手法试验旨在评估电针治疗对尿失禁患者的电针治疗的有效性和安全性。在大韩民国的2家医院将招募40岁的卒中幸存者。在2年内经历卒中的患者,并满足尿频标准> 2,患者对患者紧急规模强度或13分或更长的国际前列腺症状规模(K-IPS)的13分或更长将被识别,以及其他资格标准。患者将随机分配给治疗或对照组,分别接受10个电针或假疗法。患者和结果评估员将被蒙蔽。主要结果是基线与试验端点之间的总紧迫性和频率分数的变化。 K-IPS,关于尿失禁性尿失禁的国际咨询,尿失禁形式和尿路症状较低的症状评分将得到效果评估。每个会议后会报告不良事件。还将计算划线指数。通过双面测试,数据将以0.05显着性水平进行统计分析。

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