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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.

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.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800019371
Enrollment
Unknown
Registered
2018-11-07
Start date
2018-11-01
Completion date
Unknown
Last updated
2020-11-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

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

Sponsors

China-Japanese Friendship Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria for hospital acquired pneumonia (HAP); 2. Positive microbiological reports during hospitalization include, but are not limited to, carbapenem-resistant; 3. Enterobacter (CRE) or carbapenem-resistant Acinetobacter baumannii (CRAB); 4. For patients with a survival time of >5 days, tigecycline is included in the antibiotic regimen and its continuous use time is >= 5 days; for patients with survival time = 48 hours, tigecycline is included in the antibiotic treatment regimen and its continuous use time needs to be >= half of the total treatment time; or other patients who believe that a reasonable treatment plan; 5. For patients with a survival time of >5 days, the antibiotic treatment regimen contains polymyxin B and its continuous use time is >= 5 days; for patients with a survival time of = 48 hours, the antibiotic treatment regimen contains polymyxin B and its continuous use time should be >= half of the total treatment time; or other patients who consider a reasonable treatment plan; 6. Antibiotic dosing regimens and courses of treatment meet the requirements of this study.

Exclusion criteria

Exclusion criteria: 1. Patients who die within 48 hours of use after tigecycline or a polymyxin B-based antibiotic regimen; 2. Other reasons that researchers believe are not suitable for this study, such as antibiotic medication confusion, difficult to analyze, etc.

Design outcomes

Primary

MeasureTime frame
28-day all-cause mortality;

Secondary

MeasureTime frame
Other mortality;Ratio of treatment success and treatment failure in hospitalization;time to reach clinical stability;fever clearance time;Hospitalization time;Time to stay in the ICU;Mechanical ventilation time;Microbiological clearance rate;Discharge patients function status;The incidence of adverse reactions (normal renal function);Type of carbapenemase genotype that can be detected;

Countries

China

Contacts

Public ContactBin Cao

China-Japanese Friendship Hospital

caobin_ben@163.com+86 13911318339

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026