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Clinical Follow-up of Pregnant Subjects Undergoing NIPT

S

Sequenom

Status

Enrolling

Conditions

Pregnancy

Treatments

Device: NIPT

Study type

Observational

Funder types

Industry
Other

Identifiers

NCT04595201
SCMM-RND-111

Details and patient eligibility

About

To obtain pregnancy outcome data from patients screened for fetal genetic status using non-invasive pregnancy testing (NIPT).

Full description

To obtain pregnancy outcome data from patients screened for fetal genetic status using non-invasive pregnancy testing (NIPT) to analyze the performance of routine assay enhancements and to identify characteristics associated with adverse obstetric outcome.

Enrollment

25,000 estimated patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Subject was pregnant and received NIPT from Sequenom/Integrated Genetics
  • Subject was 18 years of age or older at the time of NIPT
  • Pregnancy outcome is available

Exclusion criteria

  • None

Trial contacts and locations

1

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Central trial contact

Kimberly Fanelli, MS, CGC

Data sourced from clinicaltrials.gov

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