Swiss registry tracks adults with congenital heart disease to uncover hidden risks
NCT ID NCT02258724
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This registry is following 5,000 adults in Switzerland who were born with heart defects. The goal is to collect data on their long-term health, including complications and treatments. By tracking these patients over time, researchers hope to better understand the challenges they face and improve future care.
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
- What this could lead to
- If successful, this registry could provide valuable insights into the long-term health and treatment needs of adults with congenital heart disease.
- What could go wrong
- This is an observational registry, not a treatment trial. It will not directly test any new therapy, and results may take years to influence clinical practice.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Basel University Hospital
RECRUITINGBasel, 4031, Switzerland
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Bern University Hospital Inselspital
RECRUITINGBern, 3010, Switzerland
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Centre Hospitalier Universitaire Vaudois CHUV
RECRUITINGLausanne, 1011, Switzerland
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Hôpitaux Universitaires de Genève HUG
RECRUITINGGeneva, 1205, Switzerland
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Kantonsspital St.Gallen
RECRUITINGSankt Gallen, 9007, Switzerland
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University Hospital Zurich
RECRUITINGZurich, 8091, Switzerland
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