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Terminated No phase listed Observational Accepts healthy volunteers

Does the Cerebroplacental Ratio (CPR) Predict Adverse Outcomes in Low Risk Pregnancies?

ClinicalTrials.gov ID: NCT03066726

Public ClinicalTrials.gov record NCT03066726. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 5:42 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Study identification

NCT ID
NCT03066726
Recruitment status
Terminated
Study type
Observational
Phase
Not listed
Lead sponsor
Rutgers, The State University of New Jersey
Other
Enrollment
580 participants

Conditions and interventions

Interventions

Not listed

Eligibility (public fields only)

Age range
18 Years to 45 Years
Sex
Female
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 14, 2017
Primary completion
May 6, 2020
Completion
May 6, 2020
Last update posted
Jan 17, 2023

2017 – 2020

United States locations

U.S. sites
6
U.S. states
2
U.S. cities
5
Facility City State ZIP Site status
Rutgers, The State University of New Jersey New Brunswick New Jersey 08901
Saint Peters University Hospital New Brunswick New Jersey 08901
Virtua Medical Group Sewell New Jersey 08080
New York Presbyterian-Queens Hospital Flushing New York 11355
Winthrop University Hospital Mineola New York 11501
Columbia University New York New York 10032

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03066726, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 17, 2023 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03066726 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →