Russian Familial Hypercholesterolemia Registry
Recruiting now
Conditions studied: Familial Hypercholesterolemia
In brief
True prevalence of FH in the Russian Federation is unknown which leads to low percentage of diagnosed and treated cases. Research is needed to determine the prevalence of FH, specific diagnostic algorithms and optimal treatment strategies. The main aim of the present study is to evaluate the extent to which FH is underdiagnosed and undertreated in the Russian Federation for reduction of cardiovascular risk related to atherosclerosis in the country. As a first step, total cholesterol (TC) and low-density lipoprotein (LDL-C) levels will be determined in a random sample from Moscow population (n=18000). It is expected that TC ≥ 7.5 mmol/L will be detected in 10% of cohort. During 2014, approximately 500 patients will pass through non-invasive clinical examination at the Russian Cardiology Research and Production Center, including patient demographics, past medical history, family history of hypercholesterolemia, physical findings, current lipid-lowering therapies, blood tests, genetic analysis, echocardiography, carotid duplex ultrasound and exercise SPECT imaging in selected cases. On the basis of the Moscow Program four major Federal Medical Centers will be involved, and FH Registry will be created as a national, multi-center initiative to screen FH patients, control their diagnosis and management, and track clinical-reported outcomes over time. Establishment of National Guidelines for the diagnosis and treatment of FH on the basis of these data and implementation those into clinical practice in different regions of Russia will allow improving patient care. As an expected outcome, this program will raise awareness and increase appropriate assessment and treatment of FH patients in Russia, leading to a timely detection of the disease and therapy initiation.
Key facts
- Study ID
- NCT02208869
- Run by
- Russian Cardiology Research and Production Center
- People needed
- 1000
- Starts
- 2014-01-01
- Expected to finish
- 2026-12-31
- Last updated by the study team
- 2022-11-02
Who can join
Age: 7 and older, up to 80. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Total cholesterol ≥7.5 mmol/L or LDL-C ≥4.9 mmol/L (pretreatment levels)
- Familial hypercholesterolemia defined as: a. Mutation in the LDL receptor and/or the ApoB gene and/or the PCSK9 gene; or b. clinical diagnosis of heterozygous FH (HeFH) according to the Dutch Lipid Network Criteria or Simon Broom Criteria
- Patients with genetic mutation of FH
You may not qualify if…
- uncontrolled primary hypothyroidism (thyroid stimulating hormone (TSH) >1.5 x upper limit of normal (ULN)),
- nephrotic syndrome and/or renal dysfunction (scrum creatinine >2.0 mg/dL or 160mmol/l, creatinine clearance <15 ml/min) at screening.
- uncontrolled diabetes mellitus (Glycated hemoglobin >8.5%)
Where it is running
- EI Chazov National Medical Research Center of Cardiology — Moscow, Russia (enrolling)
- Chelyabinsk State Medical Academy — Chelyabinsk, Russia
- Novosibirsk Research Institute of Internal Medicine, Institute of Internal Medicine Siberian Branch of the Russian Academy of Medical Sciences — Novosibirsk, Russia
- Saint-Petersburg State University and North-West State Medical University n.a. I.I.Mechnikov — Saint Petersburg, Russia
- Samara State Medical University — Samara, Russia
Full record on ClinicalTrials.gov
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