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 @ 4:15 PM
Ignite Modification Date:
2025-12-24 @ 4:15 PM
NCT ID:
NCT07191366
Eligibility Criteria:
Inclusion Criteria:
* Pregnant women with a GA between 28 weeks and 0 days and 34 weeks and 0 days who are either diagnosed with preeclampsia or PPROM or have previously given birth before 34 weeks of gestation
* Resident in the Region of Southern Denmark
* Women speaking and understanding Danish or English
* Planning to breastfeed their infants
Exclusion Criteria:
* HELLP or severe preeclampsia indicating expected induction of labour/caesarean section within a few days (According to national guidelines)
* Chorioamnionitis indicating induction of labour/caesarean section within a few days
* Women with a vaginal cerclage and PPROM
* Women taking medications contraindicating breastfeeding
* Women with prior breast reductive surgery or mastectomy
* Below 18 years of age
* Contractions to a certain extend expecting delivery within a few days
* Included in other trials, where breastfeeding is among outcomes
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT07191366
Study Brief:
Protocol Section:
NCT07191366