Multi-Omics for Maternal Health After Preeclampsia
Recruiting · NCT06340152 · Observational (researchers observe without assigning treatment) · Lead sponsor: University of California, San Diego
View the official record on ClinicalTrials.gov →What this trial is about
To develop strategies to identify postpartum women at risk for adverse cardiovascular outcomes and provide them with preventative therapies.
Who can take part
Age range
18 Years to 50 Years
Sex
Female
Healthy volunteers
Yes - healthy volunteers may be accepted
Phase
Not specified
Study type
Observational (researchers observe without assigning treatment)
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
Where it is running
1 location listed across 1 US state.
- University of California, San Diego - San Diego, California, United States