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 @ 11:46 AM
Ignite Modification Date:
2025-12-24 @ 11:46 AM
NCT ID:
NCT03598361
Eligibility Criteria:
Inclusion Criteria:
1. Diagnosed intrauterine pregnancy until week 14.
2. Single pregnancy without congenital malformations in ultrasound examination.
3. Lack of exponents threatening miscarriage (bleeding, lower abdominal pain, chorionic hematoma).
4. Lack of use of drugs affecting the mineral metabolism of the body.
5. Signing consent to participate in the study.
Exclusion Criteria:
1. Ectopic or heterotopic pregnancy.
2. Twin pregnancy (or other multiple pregnancy).
3. Obstetric load in the direction of numerous miscarriages, premature births under 34 weeks, pregnancy, fetal growth disorders (hypotrophy, macrosomia).
4. Congenital and /or genetic defects found in current pregnancy or in the patient.
5. Supply of drugs affecting the mineral metabolism of the body.
Healthy Volunteers:
True
Sex:
FEMALE
Study:
NCT03598361
Study Brief:
Protocol Section:
NCT03598361