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A Study of Pregnancy Outcomes in Congenital Heart Disease (POACHD)

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Mayo Clinic

Status

Suspended

Conditions

Congenital Heart Disease

Study type

Observational

Funder types

Other
NIH

Identifiers

NCT06678256
24-007434
5R01HL160761-04 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The purpose of this study is to determine if a biomarker assay obtained peripartum (1st-3rd trimester and post-partum) in patients with adult congenital heart disease can predict future risk of cardiovascular adverse events and determine if temporal changes in biomarkers levels throughout the peripartum period can provide a better risk prediction compared to samples taken at a single time-point.

Enrollment

100 estimated patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Congenital Heart Disease Diagnosis
  • Currently Pregnant

Exclusion criteria

  • Unable to consent

Trial contacts and locations

1

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Central trial contact

Jolene Tuchek

Data sourced from clinicaltrials.gov

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