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ClinicalTrials.gov record
Completed No phase listed Observational

Clinical Evaluation of the SEQureDx Trisomy Test in Low Risk Pregnancies

ClinicalTrials.gov ID: NCT01597063

Public ClinicalTrials.gov record NCT01597063. 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, 8:41 AM EDT

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

Official title

A Clinical Study to Evaluate the Relative Clinical Specificity Performance of the SEQureDx Trisomy Test in Pregnant Women at Low Risk for Fetal Chromosomal Aneuploidy

Study identification

NCT ID
NCT01597063
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Sequenom, Inc.
Industry
Enrollment
3,333 participants

Conditions and interventions

Interventions

  • SEQureDx Trisomy Test Device

Device

Eligibility (public fields only)

Age range
18 Years to 34 Years
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
Jun 30, 2012
Primary completion
Jan 31, 2014
Completion
Nov 30, 2015
Last update posted
Apr 19, 2016

2012 – 2015

United States locations

U.S. sites
27
U.S. states
11
U.S. cities
25
Facility City State ZIP Site status
University of South Alabama Mobile Alabama 36604-3302
New Horizon Women's Care Chandler Arizona 85224
Precision Trials Phoenix Arizona 85032
Visions Clinical Research Tuscon Tucson Arizona 85712
Descanso OBGYN Glendale California 91208
Woodglen Medical Group Glendora California 91740
White Memorial GYN/OB Medical Group Los Angeles California 91740
Fair Oaks Women's Health Pasadena California 91105
IGO Medical Group San Diego California 92121
West Coast OBGYN San Diego California 92123
Women's Health Care Research San Diego California 92123
Women's Clinical Research Vista California 92081
Hawaii Pacific Health Honolulu Hawaii 96813
University of Iowa Health Care Iowa City Iowa 52242
University of Kansas Medical Center Kansas City Kansas 66160
Spectrum Health - Maternal Fetal Medicine Grand Rapids Michigan 49503
William Beaumont Hospital Royal Oak Michigan 48073
Virtua Health Moorestown New Jersey 08057
Virtua Health Mount Holly New Jersey 08060
Jersey Shore University Medical Center Neptune City New Jersey 07753
Saint Peter's Hospital New Brunswick New Jersey 08901
Virtua Health Sewell New Jersey 08080
Virtua Health Voorhees Township New Jersey 08043
Providence Health Partners - Center for Clinical Research Dayton Ohio 45439
University of Oklahoma Health Sciences Center Oklahoma City Oklahoma 73104
Medical University of South Carolina Charleston South Carolina 29466
Magnolia OB/GYN Research Center- Recruiting Myrtle Beach South Carolina 29572

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 NCT01597063, 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 Apr 19, 2016 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01597063 live on ClinicalTrials.gov.

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