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Efficacy, safety and pharmacoeconomics of piperacillin sodium tazobactam sodium and ceftazidime and avibactam sodium in the treatment of bacterial infections in adults: a retrospective cohort study

Efficacy, safety and pharmacoeconomics of piperacillin sodium tazobactam sodium and ceftazidime and avibactam sodium in the treatment of bacterial infections in adults: a retrospective cohort study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400090373
Enrollment
Unknown
Registered
2024-09-29
Start date
2024-10-08
Completion date
Unknown
Last updated
2024-09-30

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

Conditions

Bacterial infection in adults

Interventions

Piperacillin sodium tazobactam sodium group:None
Ceftazidime and avibactam sodium group:None

Sponsors

Xi'an Honghui Hospital of Xi'an Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Admission diagnosis was complex intraperitoneal infection, community-acquired pneumonia, hospital-acquired pneumonia, Patients with ventilator-associated pneumonia and urinary tract infections; 2. Ages 18 to 85 (including 18 and 85), gender unspecified; 3. After qualified sampling, and positive bacterial culture; 4. Piperacillin sodium and tazobactam sodium or ceftazidime and avibactam sodium were used to treat bacterial infection; 5. Complete and complete case data; 6. Patients or their families give informed consent to this protocol.

Exclusion criteria

Exclusion criteria: 1. Patients with long-term systemic history of glucocorticoid administration and immune dysfunction; 2. Allergic to piperacillin sodium tazobactam sodium or ceftazidime and avibactam sodium; 3. Patients with liver, kidney, heart and other vital organ failure; 4. Medication can not complete the corresponding course of treatment, less than 3d, and does not cooperate with relevant examination, treatment or baseline information Harvester; 5. The investigator considers that there are other conditions that are not suitable for participation in clinical trials.

Design outcomes

Primary

MeasureTime frame
Assessing the difference in treatment efficacy between two groups;

Secondary

MeasureTime frame
Assessing the difference in bacterial clearance rates between two groups;Evaluate the difference in inflammatory markers, including procalcitonin, C-reactive protein, and white blood cell count, between the two groups of patients.;Assess the distribution of pathogens, pathogen culture results, and drug resistance status in the two groups of patients.;Evaluate the difference in average length of stay and pharmaceutical economics between the two groups of patients.;The incidence of adverse reactions associated with therapeutic medications.;

Countries

China

Contacts

Public ContactZhang Binfei

Xi'an Honghui Hospital of Xi'an Jiaotong University

dr_zhili@126.com+86 131 1615 4736

Outcome results

None listed

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