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