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The efficacy, population pharmacokinetics, and pharmacodynamics of piperacillin tazobactam in patients with or without liver cirrhosis infection

The efficacy, population pharmacokinetics, and pharmacodynamics of piperacillin tazobactam in patients with or without liver cirrhosis infection: A prospective observational cohort study

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400086031
Enrollment
Unknown
Registered
2024-06-24
Start date
2024-07-01
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

Infectious diseases

Interventions

Observational group:None

Sponsors

Nanjing Drum Tower Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) Admitted to Nanjing Drum Tower Hospital from December 2023 to December 2026; (2) Adult (age = 18 years old) and agree to participate in the study; (3) Clinical diagnosis of bacterial infection with clear indications of bacterial infection; (4) Use piperacillin tazobactam for anti infection treatment.

Exclusion criteria

Exclusion criteria: (1) Due to various reasons, the treatment time of piperacillin tazobactam is less than 72 hours; (2) Severe adverse reactions after the application of piperacillin tazobactam and intolerable treatment Patients; (3) Patients who are unable to monitor blood drug concentration at the designated time due to various reasons; (4) Pregnant, pregnant or breastfeeding patients; (5) Patients undergoing extracorporeal membrane oxygenation; (6) Patients undergoing artificial liver or plasma exchange; (7) After bacterial culture, it was found that the infected bacteria were patients who were resistant to piperacillin and tazobactam; (8) According to the judgment of the research team, there are other patients who are not suitable for participating in this study or may not benefit the subjects from participating in the study

Design outcomes

Primary

MeasureTime frame
Clinical efficacy at Day 7;

Secondary

MeasureTime frame
Serum concentration of Piperacillin ;Microbial eradication rate at day 7;Length of hospital stay;30-day mortality;Re-admission at Day 30;Area under curve of SIRS score within first week after receiving therapy;Adverse Events;

Countries

China

Contacts

Public ContactDayu Chen

Nanjing Drum Tower Hospital

cdy_pharmacy@njglyy.com+86 159 5191 6689

Outcome results

None listed

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