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Assessment of Patterns of Patient Reported Outcomes in Adults With Congenital Heart Disease - International Study II

NCT04902768 · View on ClinicalTrials.gov ↗

Study Summary

This is an international, cross-sectional and descriptive study that aims to investigate differences in patient-reported outcome measures (PROMs) and patient-reported experience measures (PREMs) and that aims to explore the profile and healthcare needs of adults with congenital heart diseases.

Conditions Studied

Interventions

  • OTHER This is an observational study, there is no intervention

Study Locations (20)

Other

  • Hospital San Juan De Dios De La Plata — Buenos Aires
  • Hospital de Niños — Córdoba
  • Melbourne Children's Cardiology — Melbourne
  • Vienna General Hospital — Vienna
  • Ghent University Hospital — Ghent
  • University Hospitals Leuven — Leuven
  • Princess Marina Hospital — Gaborone
  • Hospital das Clinicas da Faculdade de Medicina de Ribeirão Preto — Ribeirão Preto
  • National Heart Hospital — Sofia
  • Clinique Medical Le Jourdain — Yaoundé

California

  • University of California — San Francisco
  • Lucile Packard Children's Hospital and Stanford Health Care — Stanford

Florida

  • University of Florida Health — Gainesville

Maryland

  • Taussig Heart Center of Johns Hopkins Hospital — Baltimore

Massachusetts

  • Boston Children's / Brigham and Women's — Boston

New York

  • Mount Sinai Heart — New York

Ohio

  • Nationwide Children's Hospital — Columbus

Oregon

  • Oregon Health and Science University — Portland

Trial Details

FieldValue
Enrollment Target 8,415 participants
Start Date 2019-08-01
Est. Completion 2022-12-31

Sponsor

KU Leuven

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04902768

The ClinicalTrials.gov registry entry for NCT04902768 describes a study currently listed as completed. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 8,415 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is KU Leuven, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Congenital Heart Disease appearing as the primary indexed condition, and to 1 intervention — of which This is an observational study, there is no intervention is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT04902768 reports 20 study locations spanning 10 distinct geographic areas — top geographies include Other, California, Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT04902768 about?

NCT04902768 is a clinical study titled "Assessment of Patterns of Patient Reported Outcomes in Adults With Congenital Heart Disease - International Study II". This is an international, cross-sectional and descriptive study that aims to investigate differences in patient-reported outcome measures (PROMs) and patient-reported experience measures (PREMs) and that aims to explore the profile and healthcare needs of adults with congenital heart diseases.

What is the current status of trial NCT04902768?

This trial is currently completed. The enrollment target is 8,415 participants. The study started on 2019-08-01. Estimated completion is 2022-12-31.

What conditions does trial NCT04902768 study?

This clinical trial studies the following conditions: Congenital Heart Disease. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT04902768?

The interventions under investigation include: This is an observational study, there is no intervention (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04902768?

This trial is sponsored by KU Leuven, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT04902768 being conducted?

This trial has 20 study locations across California, Florida, Maryland, Massachusetts, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial