Vaginal Preparation and Azithromycin to Reduce Post Cesarean Infections (NCT04163679) | Clinical Trial Compass
TerminatedNot Applicable
Vaginal Preparation and Azithromycin to Reduce Post Cesarean Infections
Stopped: Enrollment issues
United States84 participantsStarted 2019-09-18
Plain-language summary
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Who can participate
Age range18 Years – 64 Years
SexFEMALE
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* full term pregnancy
* undergoing labored, non-emergent cesarean section
* patient in labor
Exclusion Criteria:
Azithromycin contraindicated:
* Known hypersensitivity to azithromycin, erythromycin, macrolides or ketolide medications.
* liver dysfunction
* Prescription medications which may interact with azithromycin, such as nelfinavir or warfarin
* A history of a cardiac dysrhythmia (irregular heartbeats)
* Known hypersensitivity to iodine
* Patients carrying fetuses with known congenital anomalies
* Immunodeficiency
* Patients who are not in labor at the time of delivery
* Non-english speaking subjects or subjects with language barriers