跳至主要内容
临床试验/ISRCTN86579667
ISRCTN86579667已完成未知

Efficacy of EPs 7630 in children with acute non-streptococcal tonsillopharyngitis

ISO Arzneimittel GmbH & Co KG (Germany)0 个研究点目标入组 78 人开始时间: 2003年3月26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
78

研究概览

简要总结

Results article in https://pubmed.ncbi.nlm.nih.gov/14526713/ (added 07/10/2021)

研究设计

研究类型
Interventional

入排标准

入选标准

  • Patients who met the following inclusion criteria were suitable for the trial:
  • 1. Age 6¿10 years, acute tonsillopharyngitis, duration of complaints less than 48 h, negative dip-and-react-test test for ß-hemolytic streptococcus and severity of symptoms =6 points
  • 2. In addition legal guardians had to sign an informed consent

排除标准

  • Not provided at time of registration

研究者

发起方
ISO Arzneimittel GmbH & Co KG (Germany)

相似试验

Efficacy of EPs 7630 in children with acute... | 临床试验