Can a national registry predict heart attacks in inherited high cholesterol?
NCT ID NCT02693548
First seen Sep 04, 2026 · Last updated Sep 04, 2026
Summary
This study follows over 4,000 people in Spain who have familial hypercholesterolaemia, an inherited condition causing very high cholesterol and early heart disease. Researchers track their cholesterol levels and any heart events, such as heart attacks or strokes, over time. The goal is to learn which factors best predict cardiovascular problems in this high-risk group, which could improve how doctors manage the condition.
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 sharpen predictions of heart attacks and strokes in people with familial hypercholesterolaemia, guiding earlier and more personalized treatment.
- What could go wrong
- As an observational registry, it cannot prove cause and effect. Results depend on self-reported follow-up data and may not apply beyond the Spanish population studied.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 4,141 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2004
- Expected to finish
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Oct 2030
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Index cases with genetic diagnosis of FH and their relatives over 15 years old with a genetic diagnosis of FH and their unaffected relatives
- Ages
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15 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Index cases with genetic diagnosis of FH and their relatives over 15 years old with a genetic diagnosis of FH and their first-degree relatives Exclusion Criteria: * Patient unwillingness
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Fundacion Hipercolesterolemia Familiar
RECRUITINGMadrid, Madrid, 28010, Spain
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