European Non-invasive Trisomy Evaluation (EU-NITE Study): Evaluation of a targeted analysis of cell free fetal DNA in maternal blood for prenatal diagnosis of fetal trisomies.

Completed

• Conditions: chromosomal aberration; trisomy; 10083624

• Registration Number: NL-OMON36065
• Lead Sponsor: eids Universitair Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 22 July 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 630

Inclusion Criteria

Singleton pregnancy with gestational age between 9 and 23 weeks, informed consent.

Exclusion Criteria

Invasive procedure performed prior to taking the blood sample, history or active significant malignancy in the mother requiring major surgery or systemic chemotherapy, language restriction with failure to understand the study information.

Study & Design

• Study Type: Observational invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>detection rate of trisomies with Tandem SNPs</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>not applicable</p><br>