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Real-Time Therapeutic Drug Monitoring on the Prescription of Imipenem/Cilastatin and Meropenem

Real-Time Therapeutic Drug Monitoring on the Prescription of Imipenem/Cilastatin and Meropenem in Underage Inpatients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800017582
Enrollment
Unknown
Registered
2018-08-05
Start date
2018-09-01
Completion date
Unknown
Last updated
2018-08-20

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

Conditions

Bacterial infection

Interventions

Group A:Real-time therapeutic drug monitoring and measurement adjustment based on monitoring results
Group B:standard-of-care

Sponsors

Xiangya Hospital, Central South University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 18 Years

Inclusion criteria

Inclusion criteria: 1. Patient aged less than 18 years old; 2. The patient is diagnosed with bacterial infection and must be treated with imipenem/cliastatin or meropenem; 3. No less than 3 days of hospitalization and no less than 5 times of treatment with imipenem/cilastatin or meropenem.

Exclusion criteria

Exclusion criteria: 1. Patients who are allergic to imipenem/Sistine or meropenem; 2. The patients whose condition is extremely critical, and it is not suitable for them to participate in this study; 3. Patients who do not agree to the study or withdraw from the study due to personal reasons.

Design outcomes

Primary

MeasureTime frame
Plasma drug concentration of imipenem;Plasma drug concentration of meropenem;

Secondary

MeasureTime frame
Clinical effects of imipenem/cilastatin;Clinical effects of meropenem;Microbiology analysis;Laboratory indexes of liver function;Safety evaluation;

Countries

China

Contacts

Public ContactTao Yin

Department of Pharmacy, Xiangya Hospital, Central South University

simon863@vip.sina.com+86 13974872856

Outcome results

None listed

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