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Clinical pharmacokinetics/pharmacodynamics of Ceftazidime-Avibactam: A multicenter, prospective, observational study

Clinical pharmacokinetics/pharmacodynamics of Ceftazidime-Avibactam: A multicenter, prospective, observational study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400082460
Enrollment
Unknown
Registered
2024-03-29
Start date
2024-04-01
Completion date
Unknown
Last updated
2024-04-01

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

Conditions

Carbapenem-resistant gram-negative bacterial infections

Interventions

Case series:None

Sponsors

Zhejiang Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1) =18 years old; 2) Patients with clinically and microbiologically confirmed CRE or CRPA infections; 3) Patients receiving intravenous Ceftazidime-Avibactam therapy; 4) Willing to participate in this study and sign the informed consent form; if the subject lacks the ability to understand or sign the informed consent form, their legal guardian will act on their behalf in the informed consent process and agree to their participation in this study.

Exclusion criteria

Exclusion criteria: 1) Patients with positive cultures for CRE or CRPA without evidence of infection (colonized patients); 2) Patients infected with CRE or CRPA resistant to Ceftazidime-Avibactam; 3) Pregnant or lactating women; 4) Patients with a Ceftazidime-Avibactam treatment duration of less than 3 days or who are allergic.

Design outcomes

Primary

MeasureTime frame
Ceftazidime-Avibactam concentration;

Countries

China

Contacts

Public ContactYunsong Yu

Zhejiang Provincial People’s Hospital

yvys119@163.com+86 138 0579 0432

Outcome results

None listed

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