首页> 外文期刊>Frontiers in Medicine >Efficacy of Electroacupuncture Therapy in Patients With Postherpetic Neuralgia: Study Protocol for a Multicentre, Randomized, Controlled, Assessor-Blinded Trial
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Efficacy of Electroacupuncture Therapy in Patients With Postherpetic Neuralgia: Study Protocol for a Multicentre, Randomized, Controlled, Assessor-Blinded Trial

机译:电针治疗患者患者治疗神经痛的疗效:多期式,随机,控制,评估综合试验的研究方案

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Introduction: The efficacy of conventional treatments for treating postherpetic neuralgia (PHN) remains unsatisfactory. Thus, this multicentre, randomized controlled, assessor-blinded trial aims to investigate the efficacy and safety of electroacupuncture (EA) therapy in patients with PHN. Methods and Analysis: This multicentre randomized controlled trial will enroll 132 patients with PHN from 3 hospitals. All patients will be randomly assigned to either the EA combined with medication group or medication group through a computerized central randomization system in a 1:1 ratio. Outcome measures will be assessed before intervention, at 2, 4, 6 weeks after intervention and at the end of 8-week follow-up. Primary outcomes will be sensory thresholds and pain intensity. Secondary outcomes will include dosage of analgetic, quality of life, anxiety, and depression severity and sleep quality. All adverse effects will be assessed during the trial. Conclusions: This study will provide evidence to ascertain whether EA is effective and safe for treating PHN. Ethics and Dissemination: Ethics approval (No.ZSLL-KY-2017-025) has been obtained from the Ethics Committee of The Third Affiliated Hospital of Zhejiang Chinese Medical University. Informed consent will be signed prior to subject enrolment. The results will be submitted to international peer-reviewed journals and presented at international conferences. Trial Registration Number: The study protocol has been registered in the clinicaltrials registry with the identification code {"type":"clinical-trial","attrs":{"text":"NCT04594226","term_id":"NCT04594226"}} NCT04594226 .
机译:介绍:治疗术治疗POSTHERPETICGIA(PHN)的疗效仍然不令人满意。因此,这种多期式,随机控制,评估综合试验旨在探讨电针(EA)治疗患者患者PHN患者的疗效和安全性。方法和分析:该多期式随机对照试验将注册来自3家医院的132名博士。所有患者将通过计算机化的中央随机化系统随机分配给EA结合药物组或药物组,在1:1的比例中。将在干预前评估结果措施,在干预后的2,4,4,4周,并在8周后的后续行动结束时进行评估。主要结果将是感觉阈值和疼痛强度。二次结果将包括患上的病毒,生活质量,焦虑和抑郁症严重程度和睡眠质量。在审判期间将评估所有不利影响。结论:本研究将提供证据,以确定EA是否有效和安全地治疗PHN。道德和传播:伦理批准(No.Zsll-Ky-2017-025)已从浙江中国医科大学第三届附属医院获得。在受试者注册之前将签署知情同意书。结果将提交给国际同行评审期刊,并在国际会议上提出。试用登记号码:研究协议已在临床节注册表中注册,识别码{“类型”:“临床 - 试验”,“attrs”:{“text”:“nct04594226”,“term_id”:“nct04594226”} nct04594226。

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