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Heart Institute Biobank & Registry for Adult Congenital Heart Disease and Related Disorders

NCT07477197 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 5000

Last updated 2026-03-17

No results posted yet for this study

Summary

A repository of biospecimens and detailed phenotypic information collected longitudinally from adults with congenital heart disease and related conditions, with an aim to facilitate future research on biologic mechanisms of underlying disease, compensation and deterioration; biologic correlates of patient experience and functional status; associations between clinical characteristics and various biomarkers; and predictors of clinical outcomes.

Conditions

  • Adult Congenital Heart Disease
  • Pulmonary Hypertension
  • Connective Tissue Disease
  • Other Cardiovascular Conditions

Sponsors & Collaborators

  • Children's Hospital Medical Center, Cincinnati

    lead OTHER

Principal Investigators

  • Sasha Opotowsky · Children's Hospital Medical Center, Cincinnati

Eligibility

Min Age
16 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-07-01
Primary Completion
2050-01-01
Completion
2050-01-01

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07477197 on ClinicalTrials.gov