Vaginal Preparation and Azithromycin to Reduce Post Cesarean Infections

Stopped early · Not applicable

Conditions studied: Infection, Obstetric Labor Complications, Endometritis, Cesarean Delivery Affecting Fetus, Wounds Injuries

In brief

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Key facts

Study ID

NCT04163679

Run by

Womack Army Medical Center

People needed

84

Starts

2019-09-18

Expected to finish

2021-07-30

Last updated by the study team

2021-10-11

Who can join

Age: 18 and older, up to 64. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• full term pregnancy
• undergoing labored, non-emergent cesarean section
• patient in labor

You may not qualify if…

• 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

Where it is running

• Womack Army Medical Center — Fort Bragg, North Carolina, United States

Full record on ClinicalTrials.gov

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