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临床试验/JPRN-UMIN000005137
JPRN-UMIN000005137已完成3 期

Examination of clinical utility of XX-45(double-balloon enteroscope) - Examination of clinical utility of double-balloon enteroscope

FUJIFILM Corporation0 个研究点目标入组 120 人开始时间: 2011年2月25日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
入组人数
120

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
13years-old 至 79years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1)Patients with acute abdomen 2)Patients with severe acute inflammation 3)Patients with anaphylaxis to natural rubber 4)Patients in a very bad general condition 5)Patients with suspected intestinal perforation 6)Patients having severe blood clotting defect 7)Patients with severe hepatic function disorder 8)Patients with severe respiratory diseases or circulatory diseases 9)Gravida and possibly pregnant patients 10)Patients who have participated in other clinical trials within 3 months prior to the start of this trial. 11)Patients who do not have the capacity or intention to cooperate with the trial procedures. 12)Patients who have experienced any adverse reactions through the enteroscopy. 13)Patients, the investigator (or the subinvestigator) considers, inappropriate for entry into the trial. 14)Sick or injured persons in life-threatening conditions and from whom it seems difficult to obtain written informed consent for their participation in the trial. 15)Patients with whom insertion of the endoscope has to be conducted via the stoma.

研究者

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