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Clinical Trials/NCT00917527
NCT00917527
Unknown
Phase 4

Randomized Placebo-controlled Crossover Trial of Endothelial Function Improvement in Subjects With History of Premature Coronary Artery Disease

Yonsei University1 site in 1 country77 target enrollmentJune 2009

Overview

Phase
Phase 4
Intervention
Atorvastatin
Conditions
Coronary Heart Disease
Sponsor
Yonsei University
Enrollment
77
Locations
1
Primary Endpoint
improvement of endothelial dysfunction with endo-PAT2000
Last Updated
13 years ago

Overview

Brief Summary

The aim of this prospective study is to investigate the prevalence of endothelial dysfunction in subjects with family history of premature coronary heart disease. At the same time, the effect of atorvastatin in treating subclinical endothelial dysfunction in those patients will be evaluated.

Registry
clinicaltrials.gov
Start Date
June 2009
End Date
June 2013
Last Updated
13 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Hyuk-Jae Chang

Yonsei University

Yonsei University

Eligibility Criteria

Inclusion Criteria

  • within 1 year
  • the siblings of premature coronary heart disease(male\<55years old, female\<65years old: Framingham Heart Study)patients admitted relevant hospital

Exclusion Criteria

  • Documented coronary heart disease
  • Any woman of childbearing potential who is pregnant, seeking to become pregnant or suspects that she may be pregnant.

Arms & Interventions

Control

Intervention: Atorvastatin

Atorvastatin

Intervention: Atorvastatin

Outcomes

Primary Outcomes

improvement of endothelial dysfunction with endo-PAT2000

Time Frame: 6 weeks later drug administration

Study Sites (1)

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