Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 7:51 PM
Ignite Modification Date:
2025-12-24 @ 7:51 PM
NCT ID:
NCT04573504
Eligibility Criteria:
Inclusion Criteria:
* 18 years old and older
* 3rd or 4th degree laceration upon delivering vaginally at Prentice Women's Hospital
* English-speaking
* Administered Ancef during wound repair
* First Delivery
* Single child being born
* Term Delivery (i.e. at least 37 weeks gestation)
Exclusion Criteria:
* Under 18 years old
* Non-English speaking
* Delivery of more than one fetus (i.e. twins or other multiples)
* Patient is taking systemic steroids
* Allergy to Amoxicillin AND Clindamycin
* Infant with severe jaundice who is receiving breastmilk
* Women who have medical contraindications to the use of metronidazole, clindamycin, and amoxicillin clavulanate.
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT04573504
Study Brief:
Protocol Section:
NCT04573504