跳至主要内容
临床试验/JPRN-UMIN000034299
JPRN-UMIN000034299已完成未知

Feasibility study investigating the efficacy and safety of SOUTEN snare for colorectal endoscopic submucosal dissection - Efficacy and safety of SOUTEN snare for colorectal endoscopic submucosal dissection

TT Medical Center Tokyo Department of Gastroenterology0 个研究点目标入组 119 人开始时间: 2018年10月1日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
119

研究概览

简要总结

Among 137 neoplasms, SOUTEN-ESD was completed in all cases. No cases required conversion to hybrid ESD or to a dedicated ESD device. The mean procedure time was about 26 minutes. The en-bloc resection rate was 100% and the R0 resection rate was 100%. The rate of perforation was 0%, the rate of delayed bleeding was 2.2%, and the rate of post-ESD coagulation syndrome (PECS) was 2.9%.

研究设计

研究类型
Observational

入排标准

年龄范围
20years-old 至 100years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • Patients whose lesions were found to be outside the guideline or expanded criteria for ESD by the endoscopic characteristics and histological findings of biopsy specimens. Patients in disagreement with informed consent

研究者

发起方
TT Medical Center Tokyo Department of Gastroenterology

相似试验