Cap-assisted endoscopic sclerotherapy for internal hemorrhoids: technique protocol and study design for a multi-center randomized controlled trial.

IF 3 Q2 GASTROENTEROLOGY & HEPATOLOGY
Therapeutic Advances in Gastrointestinal Endoscopy Pub Date : 2020-06-05 eCollection Date: 2020-01-01 DOI:10.1177/2631774520925636
Xia Wu, Quan Wen, Bota Cui, Yafei Liu, Min Zhong, Yu Yuan, Lihao Wu, Xiaoyin Zhang, Yunlian Hu, Muhan Lv, Qianneng Wu, Suyu He, Yan Jin, Shuxin Tian, Rong Wan, Xin Wang, Long Xu, Jianling Bai, Guangming Huang, Guozhong Ji, Faming Zhang
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引用次数: 7

Abstract

Background: Cap-assisted endoscopic sclerotherapy is a new interventional therapy for internal hemorrhoids and rectal prolapse under colonoscopy. The proper length of the endoscopic injection needle is the core for performing cap-assisted endoscopic sclerotherapy well with more benefits and less complications. However, no data are currently available to guide endoscopists to consider the length of injection needle before cap-assisted endoscopic sclerotherapy. This study is designed to evaluate the efficacy and safety of cap-assisted endoscopic sclerotherapy with long or short injection needle in the treatment of internal hemorrhoids.

Methods: This is a nationwide multi-center, prospective, single-blind and randomized controlled trial. Patients with grade I-II internal hemorrhoids who have failed to conservative treatments and grade III internal hemorrhoids who are not suitable for surgery or refuse surgery will be included. Participants will be randomized 1:1 into either long or short injection needle group. The primary outcome is the recurrence rate of internal hemorrhoids 24 weeks after cap-assisted endoscopic sclerotherapy. The secondary outcomes are as follows: (1) symptom severity score, (2) three-level EuroQoL five dimensions health scale scores, (3) occurrence of adverse events and severe adverse events, and (4) patients' attitudes toward cap-assisted endoscopic sclerotherapy. Data collection will be conducted before and during operation, the 1st day, 1st week, 2nd week, and 24th week after cap-assisted endoscopic sclerotherapy.

Discussion: The outcome of this study is expected to provide a practical clinical protocol of cap-assisted endoscopic sclerotherapy for patients with internal hemorrhoids and promote the use of this new endoscopic technique.

Trial registration: ClinicalTrials.gov, NCT03917056. Registered on 12 April 2019.

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帽辅助内痔内镜硬化治疗:多中心随机对照试验的技术方案和研究设计。
背景:cap辅助内镜硬化治疗是结肠镜下治疗内痔和直肠脱垂的一种新型介入治疗方法。合适的内镜注射针长度是做好帽辅助内镜硬化治疗的核心,其益处多,并发症少。然而,目前尚无数据指导内镜医师在帽辅助内镜硬化治疗前考虑注射针的长度。本研究旨在评价帽辅助内镜下长、短注射针硬化治疗内痔的疗效和安全性。方法:这是一项全国性的多中心、前瞻性、单盲、随机对照试验。I-II级内痔患者保守治疗失败,III级内痔患者不适合手术或拒绝手术。受试者按1:1随机分为注射针长组和注射针短组。主要结果是帽辅助内镜硬化治疗后24周内痔的复发率。次要结局为:(1)症状严重程度评分,(2)EuroQoL五维度健康量表三级评分,(3)不良事件和严重不良事件的发生情况,(4)患者对帽辅助内镜硬化治疗的态度。在手术前、术中、帽辅助内镜硬化治疗后第1天、第1周、第2周、第24周收集数据。讨论:本研究的结果有望为内痔患者提供一种实用的帽辅助内镜硬化治疗的临床方案,并促进这种新型内镜技术的使用。试验注册:ClinicalTrials.gov, NCT03917056。2019年4月12日注册
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来源期刊
CiteScore
4.80
自引率
0.00%
发文量
8
审稿时长
13 weeks
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