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RecruitingNCT07144839

Placental Risk Assessment to CusTomize Individualized Pregnancy Care and Evaluation

Clinical Utility of a Predictive Model of Placental Insufficiency

Status
Recruiting
Phase
Study type
Observational
Enrollment
640 (estimated)
Sponsor
Oregon Health and Science University · Academic / Other
Sex
Female
Age
15 Years – 50 Years
Healthy volunteers
Not accepted

Summary

This is a prospective observational study with the goal of developing and assessing a predictive model of placental insufficiency.

Detailed description

Pregnant study participants will be recruited and monitored throughout pregnancy with ultrasound and blood draws, and delivery and neonatal data up to 28 days following birth. This data will be used to develop a model to predict placental insufficiency.

Conditions

Interventions

TypeNameDescription
OTHERData Collection Throughout Pregnancy and DeliveryParticipants will receive monitoring by ultrasound and blood tests at three time points during pregnancy, and delivery and neonatal data will be collected.

Timeline

Start date
2025-09-18
Primary completion
2029-06-01
Completion
2029-06-01
First posted
2025-08-28
Last updated
2025-12-17

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT07144839. Inclusion in this directory is not an endorsement.

Placental Risk Assessment to CusTomize Individualized Pregnancy Care and Evaluation (NCT07144839) · Clinical Trials Directory