WHO ICTRP trial

Clinical Efficacy and Safety of the Combination of Polymyxin B plus Tigecycline…

ChiCTR1800019371 · Chinese Clinical Trial Registry (ChiCTR) · Recruiting

Key facts

Trial ID ChiCTR1800019371
Public title Clinical Efficacy and Safety of the Combination of Polymyxin B plus Tigecycline in the Treatment of hospital acquired pneumonia caused by Carbapenem-Resistant Enterobacteriaceae or Carbapenem-Resistant Acinetobacter baumannii.
Scientific title Clinical Efficacy and Safety of the Combination of Polymyxin B plus Tigecycline in the Treatment of hospital acquired pneumonia caused by Carbapenem-Resistant Enterobacteriaceae or Carbapenem-Resistant Acinetobacter baumannii.
Primary sponsor China-Japanese Friendship Hospital
Registry Chinese Clinical Trial Registry (ChiCTR)
Recruitment status Recruiting
Study type Observational study
Phase Retrospective study
Countries China
Conditions Hospital acquired pneumonia
Interventions Exposure group:Based on polymyxin B combined with Tigecycline treatment group;Control group:Treatment group based on polymyxin B;Control group:Treatment group based on Tigecycline
Registration date Nov 7, 2018
Target size Exposure group:100;Control group:150;Control group:150
Registry page chictr.org.cn

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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date:

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