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Clinical Trials/NCT01543308
NCT01543308
Unknown
Not Applicable

Phase 1 Study of Coronary Heart Disease Proteomics Research

Chinese Academy of Medical Sciences, Fuwai Hospital1 site in 1 country400 target enrollmentFebruary 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Coronary Heart Disease
Sponsor
Chinese Academy of Medical Sciences, Fuwai Hospital
Enrollment
400
Locations
1
Primary Endpoint
Differential Proteins and the levels of Differential Proteins
Last Updated
12 years ago

Overview

Brief Summary

The protein composition of HDL is complicated. The investigators have identified 40 distinct proteins associated with HDL by proteomics technology, and these proteins have been confirmed to be related to the function of anti-inflammation, anti-oxidation, improvement of endothelial function, inhibition of thrombosis and so on. And the investigators also found that the levels of some proteins in HDL changed in patients with coronary heart disease, compared with the healthy control group.

So, this study is to conduct in the two following aspects: enlarge the sample size to verify the preliminary results to find new research ideas of pathogenesis and biomarkers for coronary heart disease; and study the changes of HDL protein composition in patients with coronary heart disease before and after statins treatment using proteomics technology in order to find the mechanism of statins pleiotropic effects and indicators for evaluating the treatment effectiveness.

Registry
clinicaltrials.gov
Start Date
February 2012
End Date
December 2015
Last Updated
12 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Chinese Academy of Medical Sciences, Fuwai Hospital
Responsible Party
Principal Investigator
Principal Investigator

Yan Li-rong

Key Laboratory of Clinical Trial Research in Cardiovascular Drugs

Chinese Academy of Medical Sciences, Fuwai Hospital

Eligibility Criteria

Inclusion Criteria

  • Angiographic evidence of coronary artery disease, and no lipid-lowering therapy in the past 2 weeks for treatment group;

Exclusion Criteria

  • Use of potent lipid-lowering therapy for more than 2 weeks; myocardial infarction or percutaneous coronary intervention in the past 6 months; severe congestive heart failure, valvular heart disease and other non-coronary heart disease cardiovascular disease; liver or renal dysfunction; connective tissue disease; infection, Malignancy; and other conditions that physicians considered inappropriate to the study.

Outcomes

Primary Outcomes

Differential Proteins and the levels of Differential Proteins

Time Frame: up to 3 years

Study Sites (1)

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