Observational study on genetic lipid disorders in Italy
Official title: Lipid Transport Disorder Italian Genetic Record (LIPIGEN)
Run by Fondazione SISA (Societa Italiana per lo Studio della Arteriosclerosi) · NCT06362473 · Data updated 2026-11-12
This study looks at families with high cholesterol to see how genetics affect their condition and treatment, using information gathered during regular doctor visits.
Quick facts
| Study type | Observational |
|---|---|
| Sex | All |
| Enrollment | 15000 (estimated) |
| Sponsor | Fondazione SISA (Societa Italiana per lo Studio della Arteriosclerosi) Academic / other |
| Locations | 1 site (Sesto San Giovanni, Milano) |
| Status | Recruiting |
| Started | August 4, 2015 |
| Main results expected | December 31, 2036 |
| Study ends | December 31, 2036 |
| Registry record updated | November 10, 2026 |
| Trial ID | NCT06362473 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are individuals with a molecular or clinical diagnosis of genetic dyslipidemia.
✕Probably not a fit
Patients without a diagnosis of genetic dyslipidemia will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
LIPIGEN is an observational study that involves Italian physicians and researchers focusing on familial dyslipidaemias, particularly familial hypercholesterolaemia (FH). The study collects data from patients during their routine clinical examinations without introducing additional procedures. It aims to enhance the understanding of FH and related conditions by examining clinical diagnoses, genetic testing, and treatment effectiveness. The research also seeks to identify genetic mutations responsible for these disorders to inform more effective treatment strategies.
Why it matters
Potential benefit: If successful, this study could lead to improved diagnosis and treatment options for patients with familial hypercholesterolaemia and other genetic lipid disorders.
How similar studies have gone: Other studies focusing on genetic dyslipidemias have shown promise, but this specific observational approach is relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Molecular or clinical diagnosis of genetic dyslipidemia * Informed consent signed Exclusion Criteria: * None
Where it's running
-
IRCCS Multimedica
Sesto San Giovanni, Milano, Italy Recruiting
Study contacts
- Study coordinator: Manuela Casula, PhD
- Email: manuela.casula@unimi.it
- Phone: +390250318428
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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ORIGIN-FH: Newborn screening to detect familial high cholesterol
This project will test a genetic cheek swab of parents plus blood screening of newborns to find familial high cholesterol in babies born to parents with familial hypercholesterolemia.
-
Gene testing for diagnosing and treating heart disease
This study is trying to see if gene testing can help doctors better diagnose and treat heart conditions related to arrhythmias in patients at the Cardiogenetic Center in Italy.
-
Registry for hereditary cardiovascular diseases in Brazil
This study is trying to create a registry of Brazilian patients with hereditary heart diseases to see how common certain genetic changes are in people with these conditions.
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Exploring YOLT-101 for treating Familial Hypercholesterolemia
This study is testing a new treatment called YOLT-101 to see if it can safely lower cholesterol levels in people with familial hypercholesterolemia.
-
Atlantic program to optimize cholesterol-lowering care
This program will try coordinated outreach with primary care providers to lower LDL-C in people with familial hypercholesterolemia or LDL-C ≥160 mg/dL.
-
Improving detection of familial hypercholesterolemia through lab comments on cholesterol levels
This study is testing if adding helpful comments about high cholesterol levels in lab reports can lead to more people being referred for familial hypercholesterolemia diagnosis and treatment in Southern Denmark.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.