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Genetic Causes of Familial Hypercholesterolemia

NCT04101149 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 150

Last updated 2025-04-08

No results posted yet for this study

Summary

Familial hypercholesterolemia (FH) is a common disease. The genetic background to FH is not yet fully understood. In the present prospective cohort study we aim to study the association between different clinical characteristics, gene mutations and prognosis.

Conditions

  • Familial Hypercholesterolemia

Interventions

OTHER

No intervention

No intervention.

Sponsors & Collaborators

  • Region Örebro County

    lead OTHER

Principal Investigators

  • Anna M Nordenskjöld, MD, PhD · Örebro University, Sweden

Eligibility

Min Age
8 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-09-01
Primary Completion
2025-12-31
Completion
2045-12-31

Countries

  • Sweden

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 NCT04101149 on ClinicalTrials.gov