Expired Study
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Stanford, California 94305


Purpose:

To compare once daily versus 8 hour dosing of gentamicin for the treatment of chorioamnionitis.


Criteria:

Inclusion Criteria: - clinical diagnosis of chorioamnionitis Exclusion Criteria: - maternal renal disease, intrauterine fetal death, allergy to gentamicin


NCT ID:

NCT00185991


Primary Contact:

Principal Investigator
Yasser Yehia El-Sayed
Stanford University


Backup Contact:

N/A


Location Contact:

Stanford, California 94305
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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