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Endothelial Dysfunction in Subjects With History of Premature Coronary Artery Disease

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

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00917527
Enrollment
77
Registered
2009-06-10
Start date
2009-06-30
Completion date
2013-06-30
Last updated
2012-07-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Heart Disease

Keywords

Subjects with family history of coronary heart disease

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.

Interventions

DRUGAtorvastatin

Atorvastatin 40mg/D for 6 weeks to improve endothelial dysfunction

Sponsors

Yonsei University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frame
improvement of endothelial dysfunction with endo-PAT20006 weeks later drug administration

Countries

South Korea

Contacts

Primary ContactHyuk-Jae Chang, MD, PhD
hjchang@yuhs.ac82-2-2228-8461

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026