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ClinicalTrials.gov record
Completed No phase listed Observational

Noninvasive Screening for Fetal Aneuploidy: A New Maternal Plasma Marker

ClinicalTrials.gov ID: NCT00971334

Public ClinicalTrials.gov record NCT00971334. 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 22, 2026, 2:21 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
NCT00971334
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Sequenom, Inc.
Industry
Enrollment
2,502 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

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

Study timeline

Start date
Jul 31, 2009
Primary completion
Aug 31, 2011
Completion
Nov 30, 2011
Last update posted
Feb 16, 2012

2009 – 2011

United States locations

U.S. sites
30
U.S. states
18
U.S. cities
24
Facility City State ZIP Site status
University of South Alabama Mobile Alabama 36604-3302
Grossmont Center for Clinical Research La Mesa California 91942
IGO San Diego California 92121
San Diego Perinatal Center San Diego California 92123
Women's Healthcare at Frost Street San Diego California 92123
Poway Womens Care San Diego California 92128
Visions Clinical Research Boynton Beach Florida 33472
University of Miami Miami Florida 33136
South Florida Perinatal Medicine Miami Florida 33143
Global Ob/Gyn Centers Pembroke Pines Florida 33323
Discovery Clinical Research Sunrise Florida 33323
Sheridan Clinical Research Sunrise Florida 33323
Fetal Diagnostic Institution of the Pacific Honolulu Hawaii 96814
Women's Clinic Boise Idaho 83712
Reproductive Genetics Institute Chicago Illinois 60602
Spectrum Health - Maternal Fetal Medicine Grand Rapids Michigan 49503
William Beaumont Hospital Royal Oak Michigan 48073
Mayo Clinic Rochester Minnesota 55905
St Louis University St Louis Missouri 63117
Methodist Hospital Omaha Nebraska 68022
Cooper University Hospital Camden New Jersey 08103
Lyndhurst Gynecologic Associates Winston-Salem North Carolina 27103
Complete Healthcare for Women Columbus Ohio 43231
Clinical Trials of America Eugene Oregon 97401
Thomas Jefferson University Hospital Philadelphia Pennsylvania 19107
Medical University of South Carolina Charleston South Carolina 29425
Kingsport Perinatology Kingsport Tennessee 37660
Perinatal Research Center Nashville Tennessee 37203
Tenessee Maternal Fetal Medicine Nashville Tennessee 37203
Houston Perinatal Associates Houston Texas 77054

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00971334, 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 Feb 16, 2012 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00971334 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →