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 @ 1:19 PM
Ignite Modification Date:
2025-12-24 @ 1:19 PM
NCT ID:
NCT03608995
Eligibility Criteria:
Inclusion Criteria:
* Major pregnant women admitted to Clermont-Ferrand CHU maternity for threatened preterm delivery with intact membranes between 24 and 34 (+6 days) week of amenorrhea, with length of cervix \< 30mm (ultrasound measurement).
* Ability to give informed consent.
* French social security scheme.
Exclusion Criteria:
* \- Dilation of the cervix ≥ 4 cm
* Triple pregnancy or more
* Fetal membranes rupture
* Known uterine malformation
* Hydramnios
* Fetal malformation
* Placenta previa
* Abundant metrorrhagia
* Patient who had already participated in the study during the same pregnancy
* Patient under guardianship or curatorship
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT03608995
Study Brief:
Protocol Section:
NCT03608995