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 @ 11:13 PM
Ignite Modification Date:
2025-12-24 @ 11:13 PM
NCT ID:
NCT04140669
Eligibility Criteria:
Inclusion Criteria
• Pregnant women, aged 18 years or older, with one of the following prenatal diagnoses:
* Monochorionic diamniotic twin pregnancies complicated with TTTS
* Fetuses with CDH, but no other structural or chromosomal abnormalities
* Fetuses with NTD, but no other structural or chromosomal abnormalities
* Fetuses with LUTO, but no other structural or chromosomal abnormalities
* That provide written Informed Consent and is willing to comply with protocol requirements
Exclusion Criteria
* Presence of fetal cardiac anomalies, arrhythmias, associated morbid or lethal anomalies, chromosomal abnormalities
* Pregnancy complications that are known to impact fetal and neonatal outcomes (e.g. diabetes mellitus, hypertension, autoimmune disorders
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT04140669
Study Brief:
Protocol Section:
NCT04140669