Multi-Omics for Maternal Health After Preeclampsia
University of California, San Diego · with National Human Genome Research Institute (NHGRI), Vanderbilt University Medical Center · NCT06340152
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18–50 · Women only
- Healthy volunteers
- Accepted
- Study type
- Observational
- Target enrollment
- 1100
- US sites recruiting
- 1
- Study start
- December 20, 2023
- Record last updated
- April 6, 2025
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
To develop strategies to identify postpartum women at risk for adverse cardiovascular outcomes and provide them with preventative therapies.
Conditions: Pre-Eclampsia; Pregnancy Induced Hypertension
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Pregnant women 18 years of age to 50 years of age
- 10-24 weeks gestation at time of enrollment
- Singleton pregnancy
- Planning to deliver at a study site (UCSD or VUMC)
Exclusion Criteria
- Inability to give informed consent
- Intrauterine fetal demise
- Fetal genetic or structural anomaly
- Institutionalization for psychiatric disorder, mental deficiency or incarcerated
- Active or history of malignancy requiring major surgery or systemic chemotherapy
- Multi-fetal gestation or a twin demise at any gestational age
- Known maternal or fetal chromosomal anomalies
- Patients who plan to keep their placenta after delivery
Recruiting US locations
University of California, San Diego
San Diego, CA 92037
Site contact: Maya Selvaraj · 858-776-8374 · mlselvaraj@health.ucsd.edu
Study contacts (from the official record)
- Maya Selvaraj · 858-249-5985 · momhealthstudy@health.ucsd.edu
- Valentina Stanley · 858-249-5985
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