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临床试验/KCT0009050
KCT0009050已完成Unknown

A Prospective, Multi-national, Multicenter, Randomized Controlled Trial to Evaluate Safety and Effectiveness of Endoscopic Hemostatic Powder, ‘Nexpowder’ for Hemostatic Treatments of Nonvariceal, Upper Gastrointestinal Bleeding

extbiomedical0 个研究点目标入组 352 人开始时间: 待定最近更新:
适应症

试验速览

阶段
Unknown
状态
已完成
发起方
入组人数
352

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
19(Year) 至 o Limit(—)
性别
All

入选标准

  • 1.Males or females of Age of 19 (Nineteen) or Older
  • (In case of Age of 75 (Seventy-Five) or older or if patient falls under emergencycondition, a written consent from the patient's guardian or legal representativeis required)
  • 2.Indication of non-variceal upper gastrointestinal bleeding.
  • 3.Forrest scores Ia, Ib or IIa by endoscopy findings
  • (Patients with class IIb or adherent clot, were reevaluated for class Ia, Ib or IIa after intensive irrigation procedure was performed to remove the clot)
  • 4.Subjects who voluntarily agreed to the clinical trial and who were willing toand could comply with the study protocol

排除标准

  • 1.Patients, who are unable to receive endoscopic treatment due to comorbidity
  • 2.The 30-day follow-up is not possible.
  • 3.Patients who are going through Pregnancy or breastfeeding
  • 4.Endoscopic treatment is prohibited because of comorbidity
  • 5.Patients who participated in the related clinical trials that can affect the studyresults within the past month
  • 6.Other cases in which participation in the study is not appropriate by thejudgment of the investigators

研究者

发起方
extbiomedical

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