跳至主要内容
临床试验/JPRN-UMIN000033255
JPRN-UMIN000033255已完成未知

Pilot Study of efficacy and safety of nalfurafine hydrochloride for jaundice associated pruritus - Pilot Study of efficacy and safety of nalfurafine hydrochloride for jaundice associated pruritus

Wakayama Medical University0 个研究点目标入组 12 人开始时间: 2018年7月4日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
12

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
20years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • Patient's consciousness are not alert. Presence of hypersensitivity to nalfurafine hydrochloride and/or fexofenadine hydrochloride. Presence of other dermatosis except for jaundice associated pruritis. Presence of sever organopathy and/or drug allergy. Patients who pregnant or possibility of pregnant, lactating and desire for childbearing. Difficult to ingestion. Ineligible cases are judged by researchers.

研究者

相似试验

Pilot Study of efficacy and safety of nalfurafine... | 临床试验