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:
2025-12-25 @ 1:38 AM
Ignite Modification Date:
2025-12-25 @ 1:38 AM
NCT ID:
NCT03570294
Eligibility Criteria:
Inclusion Criteria:
* pregnant women between 24-35 weeks' gestation receiving prenatal care due to the risk of premature birth
* intact membranes
* evidence of premature labor (regular, painful and persistent uterine contractions; cervical changes)
Exclusion Criteria:
* acute fetal distress
* other conditions requiring immediate delivery (eclampsia and severe pre-eclampsia, placenta previa, abruptio placenta)
* vaginal bleeding,
* premature rupture of membranes
* chorioamnionitis,
* fetal congenital malformations,
* intrauterine growth restriction,
* the use of any tocolytic drugs during pregnancy before admission to the hospital
* circulatory system diseases (e.g. heart defects, hypertension),
* symptoms of infection
* other diseases that may increase oxidative stress
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
45 Years
Study:
NCT03570294
Study Brief:
Protocol Section:
NCT03570294