Study identifier:NIS-CRU-DUM-2010/1
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
Centralized pan-Russian Survey on the undertreatment of hypercholesterolemia
dyslipidaemia
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No
-
All
1000
Observational
18 Years +
Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Jan 2015 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
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The purpose of the study is to establish the proportion of patients on lipid-lowering pharmacological treatment reaching the LDL-C goals according to the All-Russian Scientific Cardiology Society guidelines/ the 4th Joint European Task Force guidelines.
Location
Location
Krasnodar, Russian Federation
Location
Moscow, Russian Federation
Location
Nizhniy Novgorod, Russian Federation
Location
Novosibirsk, Russian Federation
Location
Saint-Petersburg, Russian Federation
Location
Samara, Russian Federation
Location
Voronezh, Russian Federation
Location
Yaroslavl, Russian Federation
Arms | Assigned Interventions |
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1 Subject 18 years of age or older on lipid lowering drug treatment for at least 3 months, with no dose change for a minimum of 6 weeks.. | - |
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