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 @ 1:34 AM
Ignite Modification Date:
2025-12-25 @ 1:34 AM
NCT ID:
NCT02357394
Eligibility Criteria:
Inclusion Criteria:
* singleton
* cervical length \< 25 mm measured by transvaginal ultrasound prior to 23 weeks 0 days
* agrees to refrain from sexual intercourse
Exclusion Criteria:
* major fetal anomalies
* painful regular uterine contractions
* active vaginal bleeding
* ruptured membranes
* evidence of chorioamnionitis or other maternal/fetal infectious morbidity
* placenta previa
* cervical cerclage in situ
* visual cervical dilation of 2 cm or greater with visible amnion/chorion
* significant maternal-fetal complications (chronic hypertension, insulin dependent diabetes mellitus, systemic lupus erythematosus with nephritis, chronic hypertension, red cell alloimmunization, drug abuse)
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
45 Years
Study:
NCT02357394
Study Brief:
Protocol Section:
NCT02357394