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Pharmacokinetics and Pharmacodynamics and Selected Antibiotics During Pregnancy

Completed
Conditions
Pregnancy
Interventions
Registration Number
NCT00214331
Lead Sponsor
University of Wisconsin, Madison
Brief Summary

This protocol is a prospective, open-label, multicenter, population pharmacokinetic and pharmacodynamic study of selected anti-infective agents in pregnant women being treated for suspected or documented infections.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
150
Inclusion Criteria
  • Women in their second or third trimester of pregnancy
  • Women currently receiving treatment or whose physician has made the decision to start treatment with ciprofloxacin, azithromycin or gentamicin for a suspected or documented infection
  • Of childbearing potential and who either have never been pregnant or whose most recent pregnancy ended 3 months previously (control group)
  • Women greater than 3 months postpartum and currently breast-feeding (substudy)
Exclusion Criteria
  • Women with significant gastrointestinal disease which may be expected to interfere with the absorption of the orally administered anti-infective agents

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
2azithromycinazithromycin
3gentamicingentamicin
1ciprofloxacinciprofloxacin
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Wisconsin

🇺🇸

Madison, Wisconsin, United States

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