PRECEDE (Cesarean C-Section Delivery) - Clinical Trial
What is the Purpose of this Study?
Estamos realizando este estudio para determinar si la adición de azitromicina a la terapia preventiva antibiótica única de rutina puede reducir el riesgo de desarrollar infecciones después de un parto por cesárea.
Cesarean [C-Section] Delivery
Who Can Participate in the Study?
Adultos de 18+ años que están embarazadas y tendrán un parto por cesárea programado en Duke University Hospital.
For more information, contact the study team at jennifer.ferrara@duke.edu.
What is Involved?
If you choose to join this study, you will get a random assignment (like a coin flip) to receive either azithromycin or placebo (normal saline) through your existing intravenous (IV) line that is placed before you have your baby. Study participation starts when you come to the hospital to deliver your baby and will end approximately 6 weeks after delivery.
Study Details
