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临床试验/JPRN-UMIN000031921
JPRN-UMIN000031921已完成未知

A preliminary study of the effects of a new oral mucosa protective material on chemotherapy- and/or radiation-induced oral mucositis - A preliminary study of a new oral mucosa protective material

ational Cancer Center Hospital0 个研究点目标入组 10 人开始时间: 2018年3月30日最近更新:

试验速览

阶段
未知
状态
已完成
入组人数
10

研究概览

简要总结

Compared to baseline, the mean NRS began to decrease at 5 mins after using Episil ,and this effect lasted up to 120 minutes. The protective effects of Episil were observed already 3 to 5 minutes after application.Some patients felt slight soreness or discomfort when applying Episil.

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

  • 1) Patients have tumor region inside oral cavity 2) Patients have severely injured area not due to oral mucositis 3) Patients who are known or suspected CNS tumor, metastasis or invasion to the CNS 4) Patients have started the rescue medications on Day 1 prior to the application of episil(r). 5) Patients who are participating in other clinical trials 6) Female patients who are breast-feeding, pregnancy or planned pregnancy 7) Patients with considerable concern for compliance with the protocol, in the judgment of investigator

研究者

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