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 @ 11:35 PM
Ignite Modification Date:
2025-12-24 @ 11:35 PM
NCT ID:
NCT00139256
Eligibility Criteria:
Inclusion Criteria:
* Pregnant women \>/= 34 weeks gestation scheduled to undergo operative delivery within 48-72 hours after study enrollment
Exclusion Criteria:
* Known contraindication to the use of betamethasone in the mother
* Known lethal or non-lethal congenital anomaly diagnosed antenatally
* Spontaneous labor
* Premature rupture of membranes
Healthy Volunteers:
True
Sex:
FEMALE
Study:
NCT00139256
Study Brief:
Protocol Section:
NCT00139256