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Pilot study of low- vs. high-dose Rosuvastatin in minor heart attack patients and healthy controls: assessment of skin microvascular blood flow.

Phase 4
Withdrawn
Conditions
Peripheral microvascular dysfunction in non-ST segment elevation myocardial infarction (NSTEMI).
Cardiovascular - Coronary heart disease
Registration Number
ACTRN12613000575730
Lead Sponsor
yell McEwin Hosptial Department of Cardiology
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Withdrawn
Sex
All
Target Recruitment
36
Inclusion Criteria

Post-menopausal women (STRAW +10 definition) and age-matched men

NSTEMI group only - Evidence of NSTEMI: Electrocardiographic ST-segment depression or prominent T-wave inversion and/or positive biomarkers of necrosis (e.g., troponin) in the absence of ST-segment elevation and in an appropriate clinical setting (chest discomfort or anginal equivalent)

Exclusion Criteria

Current statin therapy
Skin pathology on volar forearms
Previous myocardial infarction or coronary artery bypass grafting
Known serious or hypersensitivity reactions to statin, anti-platelet agents (aspirin or clopidogrel), or heparin
Cardiogenic shock or symptomatic hypotension or sitting SBP < 95mmHg
Congestive heart failure (NYHA Class III or IV) or LVEF < 35%
Inability to provide informed consent
Non-English speaking

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Change in peripheral subcutaenous microvascular reactivity as assessed by laser Doppler flowmetry.[After 7 days Rosuvastatin treatment.]
Secondary Outcome Measures
NameTimeMethod
Percent change in blood low-density lipoprotein (LDL) levels.[After 7 days Rosuvastatin treatment.]
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