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帽辅助内镜下内痔硬化治疗:多中心随机对照试验的技术方案与研究设计

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

作者信息

Wu Xia, Wen Quan, Cui Bota, Liu Yafei, Zhong Min, Yuan Yu, Wu Lihao, Zhang Xiaoyin, Hu Yunlian, Lv Muhan, Wu Qianneng, He Suyu, Jin Yan, Tian Shuxin, Wan Rong, Wang Xin, Xu Long, Bai Jianling, Huang Guangming, Ji Guozhong, Zhang Faming

机构信息

Medical Center for Digestive Diseases, Second Affiliated Hospital of Nanjing Medical University, Nanjing, China.

Department of Gastroenterology, First Affiliated Hospital of Guangdong Pharmaceutical University, Guangzhou, China.

出版信息

Ther Adv Gastrointest Endosc. 2020 Jun 5;13:2631774520925636. doi: 10.1177/2631774520925636. eCollection 2020 Jan-Dec.

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.

摘要

背景

帽辅助内镜下硬化治疗是一种在结肠镜检查下治疗内痔和直肠脱垂的新介入疗法。内镜注射针的合适长度是成功实施帽辅助内镜下硬化治疗并获得更多益处和更少并发症的关键。然而,目前尚无数据可指导内镜医师在帽辅助内镜下硬化治疗前考虑注射针的长度。本研究旨在评估使用长或短注射针进行帽辅助内镜下硬化治疗内痔的疗效和安全性。

方法

这是一项全国多中心、前瞻性、单盲随机对照试验。纳入经保守治疗无效的Ⅰ-Ⅱ度内痔患者以及不适合手术或拒绝手术的Ⅲ度内痔患者。参与者将按1:1随机分为长注射针组或短注射针组。主要结局是帽辅助内镜下硬化治疗24周后内痔的复发率。次要结局如下:(1)症状严重程度评分;(2)欧洲五维健康量表三级评分;(3)不良事件和严重不良事件的发生情况;(4)患者对帽辅助内镜下硬化治疗的态度。数据收集将在手术前、手术期间、帽辅助内镜下硬化治疗后第1天、第1周、第2周和第24周进行。

讨论

本研究结果有望为内痔患者提供实用的帽辅助内镜下硬化治疗临床方案,并促进这种新内镜技术的应用。

试验注册

ClinicalTrials.gov,NCT03917056。于2019年4月12日注册。

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