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 @ 5:18 PM
Ignite Modification Date:
2025-12-24 @ 5:18 PM
NCT ID:
NCT06882850
Eligibility Criteria:
Inclusion Criteria: - Singleton pregnancy
* Patients attending prenatal consultations at the Obstetrics Service A of CHUC, with the first consultation occurring before 14 weeks of gestation
* Gestational age determined by first-trimester ultrasound
* Study group: Women classified as high risk for PE according to clinical/historical criteria and the Fetal Medicine Foundation algorithm. LDA-naïve.
Exclusion Criteria: Multiple pregnancy
* Autoimmune diseases
* Prior use of LDA or other immunomodulatory medication before potential recruitment
* History of spontaneous miscarriages and/or medical termination of pregnancy
* Fetal malformation
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT06882850
Study Brief:
Protocol Section:
NCT06882850