首页> 外文OA文献 >Cap-assisted endoscopic sclerotherapy for internal hemorrhoids: technique protocol and study design for a multi-center randomized controlled trial
【2h】

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

机译:用于内痔的CAP辅助内镜疗法:技术协议和用于多中心随机对照试验的研究设计

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

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.
机译:背景:CAP辅助内窥镜硬化疗法是结肠镜检查下内痔和直肠脱垂的新介入治疗。内窥镜注射针的适当长度是用于进行帽辅助内窥镜硬化疗法的核心,其良好的益处和更少的并发症。但是,目前没有数据目前无法引导内窥镜手,以考虑注射针的长度,在CAP辅助内窥镜疗法中。本研究旨在评估帽辅助内镜疗法的疗效和安全性,在内痔的治疗中具有长或短注射针。方法:这是全国范围的多中心,前瞻性,单盲和随机对照试验。患有I-II级内痔的患者未能保守治疗和不适合手术或拒绝手术的III级内痔。参与者将在长或短注射针组中随机1:1。主要结果是CAP辅助内镜疗法后24周内痔疮的复发率。二次结果如下:(1)症状严重程度,(2)三级欧元季度五维维度分数,(3)发生不良事件和严重不良事件,(4)患者对CAP辅助的态度内窥镜核发生疗法。数据收集将在运营前和期间进行,第1天,第1周,第2周和第2周和第24周辅助内窥镜疗法后第24周进行。讨论:该研究的结果预计将为内痔患者提供概率辅助内镜疗法的实用临床方案,促进使用这种新的内窥镜技术。试验注册:ClinicalTrials.gov,NCT03917056。注册于2019年4月12日。

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号