跳至主要内容
临床试验/JPRN-UMIN000031986
JPRN-UMIN000031986已完成未知

Evaluation of palatability of newly developed fast disintegrating tablet of Kremezin in patient. - Evaluation of palatability of Kremezin tablet.

School of Pharmaceutical Sciences University of Shizuoka0 个研究点目标入组 50 人开始时间: 2018年3月30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
50

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
20years-old 至 80years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • Patients who apply to administration contraindications in the package insert of kremezin Patients who will not see the outpatients clinic within 2 weeks to 2 months Patients who can not communicate due to cognitive deterioration Patients who do not manage medication by themselves and their families Patients who it is hard to swallow Patients who have extraordinary state in oral cavity. Patients who is considered as imappropriate by doctor.

研究者

发起方
School of Pharmaceutical Sciences University of Shizuoka

相似试验