Population Pharmacokinetic of Piperacillin/Tazobactam in Maternal and Neonatal Populations

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18+
SponsorShandong University

About this trial

The purpose of this study is to describe the population pharmacokinetic characteristics of piperacillin/tazobactam after intravenous administration in pregnant women during pregnancy and delivery, and to evaluate pharmacodynamic effectiveness and safety of piperacillin/tazobactam in pregnant women whose baby are at high risk of developing early-onset sepsis after birth.

Eligibility criteria

Qualifiers

Patients over 18 years old;

Pregnant women whose baby are at high risk of developing early-onset sepsis after birth have indications to use preventive or therapeutic antibiotics, and the antibiotics used are PIP/TAZO;

Patients and their families are fully aware of the research content and sign the informed consent form.

Disqualifiers

Intolerance or serious adverse reactions to antibiotic use;

Patients who stopped using PIP/TAZO more than 24 hours before delivery;

Receiving other systemic trial drugs;

There are other factors that the researchers think are not suitable for inclusion

Trial design

Treatments tested in this trial

  • Piperacillin Sodium and Tazobactam Sodium for Injection

Treatment groups

No treatment groups listed

Sponsors and collaborators

Shandong University

Lead sponsor

Shandong Provincial Hospital

Collaborator