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临床试验/ISRCTN38391551
ISRCTN38391551已完成4 期

Safety and efficacy of Sumamed® therapy in the treatment of respiratory tract infections in adults and children: international, multicentre, non-comparative study

PLIVA Hrvatska d.o.o (Croatia)0 个研究点目标入组 2,000 人开始时间: 2008年9月22日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
2,000

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

性别
All

入选标准

  • 1. Male or female out-patients, no age limits
  • 2. Acute onset of disease indicated by presence of fever (>37°C)
  • 3. Presence of at least 2 specific clinical signs and symptoms
  • 4. Signed informed consent (for minors, parent or legal guardian written consent needs to be obtained)

排除标准

  • 1. Hypersensitivity to macrolides
  • 2. Treatment with any antibiotic within 14 days prior to enrolment
  • 3. Participation in any clinical study within 4 weeks prior to enrolment
  • 4. Prior enrolment in this study

研究者

发起方
PLIVA Hrvatska d.o.o (Croatia)

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