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 @ 2:09 AM
Ignite Modification Date:
2025-12-25 @ 2:09 AM
NCT ID:
NCT02331160
Eligibility Criteria:
Inclusion Criteria:
* Understands Danish in writing.
* Intention of accepting vaginal delivery if cephalic presentation.
* Can be offered standard treatment of external cephalic version according to local guidelines, e.g.:
* Singleton pregnancy
* Fetus in breech or transverse position
* The gestational age at randomization must be between 35w+0/7d and 37w+4/7d so that the ECV is no later than 38w+0/7d for parous and 37w + 0/7d for nulliparous women.
Exclusion Criteria:
* Women that cannot be offered external cephalic version according local guideline, e.g.:
* placenta praevia and vasa praevia.
* Suspicion of severe fetal growth restriction.
* Severe preeclampsia.
* Uterus anomalies.
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT02331160
Study Brief:
Protocol Section:
NCT02331160