bacterial vaginosis
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Patients receiving trans-vaginal chloramphenicol during pregnancy for bacterial vaginosis 2.Patients receiving written informed consent
Exclusion criteria
Exclusion criteria: 1.Patients discontinued trans-vaginal chloramphenicol 2.Patients having severe kidney dysfunction or liver dysfunction
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Maternal plasma concentration of chloramphenicol | — |
Secondary
| Measure | Time frame |
|---|---|
| Factors determining the plasma exposure of chloramphenicol Effect of maternal plasma concentration of chloramphenicol on her infants | — |
Countries
Japan
Contacts
Hamamatsu University School of Medicine Department of Hospital Pharmacy