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Population pharmacokinetics study of polymyxin E sodium mesylate

Population pharmacokinetics study of polymyxin E sodium mesylate

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300072099
Enrollment
Unknown
Registered
2023-06-02
Start date
2023-06-20
Completion date
Unknown
Last updated
2023-06-12

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

Conditions

Infection of drug-resistant gram-negative bacteria

Interventions

Group of patients infected with gram-negative bacteria:None

Sponsors

Department of Pharmacy, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Age =18 years old (2) Patients infected with gram-negative bacteria (3) Patients treated with polymyxin E sodium mesylate

Exclusion criteria

Exclusion criteria: (1) Patients with polymyxin E sodium mesylate allergy (2) Pregnant women

Design outcomes

Primary

MeasureTime frame
Blood concentrations of Polymyxin E sodium mesylate;

Countries

China

Contacts

Public ContactLiu Dong

Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology

ld2069@outlook.com027-83663643

Outcome results

None listed

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