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 @ 4:12 PM
Ignite Modification Date:
2025-12-24 @ 4:12 PM
NCT ID:
NCT02530866
Eligibility Criteria:
Inclusion Criteria:
* maternal age between 18-45 years
* singleton birth
* planned delivery at OU Medical Center
* GDM diagnosed between 12-32 weeks' gestation by either a 50 gram
* one hour GCT \>200 mg/dL or two or more abnormal values on a 100 gram OGTT using the Carpenter-Coustan criteria
* pre-pregnancy BMI ≥26 kg/m2.
Exclusion Criteria:
* maternal tobacco use
* planned delivery prior to 34 weeks of gestation
* significant fetal anomalies
* chronic hypertension requiring medication
* other vascular disease
* known renal disease with a baseline serum creatinine \>1.5 mg/dL
* maternal rheumatologic disorders requiring medication
* maternal human immunodeficiency virus (HIV) or hepatitis
* as the specimen storage facility is not accredited to handle such samples
* steroid use within 7 days.
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
45 Years
Study:
NCT02530866
Study Brief:
Protocol Section:
NCT02530866