Actively Recruiting

All Genders
ID06362473

Lipid Transport Disorder Italian Genetic Record (LIPIGEN) Observational Study for Familial Hypercholesterolemia and Genetic Dyslipidemias

Led by Fondazione SISA (Societa Italiana per lo Studio della Arteriosclerosi) · Updated on 2024-04-12

10000

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are conducting the LIPIGEN observational study to better understand diseases related to blood lipid levels, such as familial hypercholesterolaemia (FH) and other genetic dyslipidaemias. The study involves Italian physicians and researchers who aim to improve diagnosis and treatment by collecting detailed patient information and analyzing genetic causes. This research may help identify the most effective treatments and monitor long-term health outcomes. Participants continue their usual clinical care while the study collects data from their medical records, family history, and genetic testing without adding extra procedures. In some cases, additional evaluations like ultrasounds may be performed to better assess the condition. The study involves more than 50 centers across Italy, making it accessible to many individuals with these conditions. Throughout the study, researchers will evaluate patients' lipid and genetic profiles at baseline and observe treatment adherence, cardiovascular events, and other important health outcomes over time. Participants' involvement includes regular clinical visits and data collection as part of standard care. The study began in 2015 and will continue through 2026, aiming to enhance personalized diagnosis and treatment strategies for genetic lipid disorders.

CONDITIONS

Brief Title

Lipid Transport Disorder Italian Genetic Record (LIPIGEN)

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Molecular or clinical diagnosis of genetic dyslipidemia
  • Signed informed consent
Not Eligible

You will not qualify if you...

  • None

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Diagnostic Evaluation

Duration - Baseline evaluation

Participants undergo evaluations to assess their lipid and genetic profiles.

1 visit (in-person)

Long-term Monitoring

Duration - Ongoing until study completion

Participants are observed to collect data related to lipid-lowering treatments and genetic dyslipidemias.

Trial Site Locations

Total: 1 location

1

IRCCS Multimedica

Sesto San Giovanni, Milano, Italy, 20099

Actively Recruiting

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Research Team

M

Manuela Casula, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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Published Research Related To This Trial