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临床试验/ISRCTN03930168
ISRCTN03930168已完成不适用

Efficacy of EPs 7630 in acute non-streptococcal tonsillopharyngitis

ISO Arzneimittel GmbH & Co KG (Germany)0 个研究点目标入组 60 人开始时间: 2002年6月14日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
60

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

入选标准

  • The study took place between March and April 1997. It is terminated. Patients, who met the following inclusion criteria, were suitable for the trial:
  • 1. Age 6-10 years
  • 2. Acute exsudative tonsillopharyngitis
  • 3. Duration of symptoms less than 48 h
  • 4. No Group A Beta Hemolytic Streptococcus (GABHS)-infection
  • 5. Tonsillopharyngitis Severity Score (TSS) 6 or more points, and
  • 6. Informed consent in writing by legal guardians who were able to understand the nature, meaning and consequences of the trial

排除标准

  • Not provided at time of registration

研究者

发起方
ISO Arzneimittel GmbH & Co KG (Germany)

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