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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00906451
Other study ID # Simvastatin Post-MI
Secondary ID
Status Completed
Phase Phase 4
First received May 19, 2009
Last updated June 21, 2011
Start date November 2008
Est. completion date May 2009

Study information

Verified date May 2009
Source Brasilia Heart Study Group
Contact n/a
Is FDA regulated No
Health authority Brazil: National Committee of Ethics in Research
Study type Interventional

Clinical Trial Summary

During myocardial infarction, inflammatory response may negatively influence ventricle wall remodeling as well as endothelium-dependent vasomotor function in the coronary and systemic arterial systems. Statins have been consistently proved to attenuate inflammation and improve endothelial function. In this study, we tested the effect of different doses of statin on inflammatory response and endothelium-dependent vasodilation.


Description:

During acute coronary syndromes (ACS), the generation of inflammatory mediators negatively influences arterial wall remodeling and the endothelium-dependent vasomotor function in the coronary and systemic arterial systems. The intensity of this inflammatory upregulation is strongly related to the incidence of recurrent coronary events. High dose potent statins can rapidly reduce plasma levels of cholesterol-rich lipoproteins and inflammatory activity in subjects during ACS. By inference, it is plausible to hypothesize that these effects during the acute phase of myocardial infarction may influence the post-discharge endothelial dysfunction. So far, data is unavailable to verify this assumption or to define the potency required for such statin anti-inflammatory effect in myocardial infarction patients. The present study aim to investigate the role of statin dose on the time-course of the inflammatory response during the acute phase of myocardial infarction and its late effect on endothelium-dependent arterial dilation.


Recruitment information / eligibility

Status Completed
Enrollment 58
Est. completion date May 2009
Est. primary completion date May 2009
Accepts healthy volunteers No
Gender Both
Age group 45 Years to 70 Years
Eligibility Inclusion Criteria:

- Less than 24 hours after the onset of MI symptoms

- ST-segment elevation of a least 1 mm (frontal plane) or 2 mm (horizontal plane) in two contiguous leads

- Myocardial necrosis, as evidenced by increased CK-MB and troponin levels

Exclusion Criteria:

- Use of statins for at least 6 months prior the myocardial infarction

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention


Intervention

Drug:
Simvastatin
Simvastatin

Locations

Country Name City State
Brazil Hospital de Base do Distrito Federal Brasilia DF

Sponsors (1)

Lead Sponsor Collaborator
Brasilia Heart Study Group

Country where clinical trial is conducted

Brazil, 

References & Publications (1)

Sposito AC, Santos SN, de Faria EC, Abdalla DS, da Silva LP, Soares AA, Japiassú AV, Quinaglia e Silva JC, Ramires JA, Coelho OR. Timing and dose of statin therapy define its impact on inflammatory and endothelial responses during myocardial infarction. A — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Elevation of plasma C reactive protein Changes in CRP levels between the first and fifth day after myocardial infarction Five days No
Secondary Brachial Artery Endothelial function 30 days No
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