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Completed No phase listed Observational

Verification of Risk Assignment for Whole Chromosome Using SNP-based NIPT in Vanishing Twin Pregnancies

ClinicalTrials.gov ID: NCT05004337

Public ClinicalTrials.gov record NCT05004337. 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 Oct 22, 2026, 5:57 PM EDT

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

Official title

Verification of Risk Assignment for Whole Chromosome Using SNP-based NIPT in Vanishing Twin Pregnancies (VANISH)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to collect blood samples from women carrying a vanishing twin pregnancy to further develop Natera's non-invasive prenatal screening test to provide information about possible chromosomal conditions for the living twin

Study identification

NCT ID
NCT05004337
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Natera, Inc.
Industry
Enrollment
136 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 22, 2021 (Actual)
Primary completion
Nov 29, 2023 (Actual)
Completion
Nov 29, 2023 (Actual)
Last update posted
Aug 17, 2026

2021 – 2023

United States locations

U.S. sites
21
U.S. states
12
U.S. cities
18
Facility City State ZIP Site status
Center for Fetal Medicine & Women's Ultrasound Los Angeles California 90048 —
Stanford Palo Alto California 94304 —
University of Colorado Aurora Colorado 80045 —
Yale New Haven Connecticut 06511 —
Christiana Care Newark Delaware 19718 —
Emerald Coast ObGyn Panama City Florida 32405 —
University of Kansas Kansas City Kansas 66160 —
University of Michigan Ann Arbor Michigan 48109 —
Beaumont Royal Oak Michigan 48073 —
Mayo Clinic Rochester Minnesota 55905 —
Hackensack Neptune City New Jersey 07753 —
St. Peter's University Hospital New Brunswick New Jersey 08901 —
NYU Long Island Mineola New York 11501 —
NYU Langone New York New York 10022 —
Icahn School of Medicine at Mount Sinai Hospital New York New York 10029 —
Columbia University New York New York 10032 —
Weill Cornell Medicine New York New York 10065 —
Montefiore Medical Center The Bronx New York 10461 —
Lehigh Valley Health Network Allentown Pennsylvania 18103 —
University of Pennsylvania Philadelphia Pennsylvania 19104 —
Cedar Health Research Irving Texas 75039 —

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 NCT05004337, 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 Aug 17, 2026 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05004337 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →