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Effect of Propolis in patients with Angina

Not Applicable
Recruiting
Conditions
Angina pectoris
Registration Number
RBR-876w38c
Lead Sponsor
Hospital Ana Nery
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
Not specified
Inclusion Criteria

Patients older than 18 years; with stable coronary artery disease (CAD) symptomatic of angina despite optimized clinical treatment for at least four weeks with antianginal drugs (beta-blockers; calcium channel blockers; nitrates and/or trimetazidine)

Exclusion Criteria

Patients scheduled for surgical or percutaneous myocardial revascularization within the next 30 days; patients with obstruction of the left main coronary artery greater than 50%; patients who had acute coronary syndrome in the last two months; electrocardiogram at rest with left bundle branch block (LBBB), Wolff-Parkinson White (WPW), pacemaker rhythm, ST-segment depression more than 1mm, digitalis therapy; patients who have some physical limitation that make it impossible to perform the exercise test on a treadmill; heart failure with symptomatic reduced ejection fraction NYHA III-IV

Study & Design

Study Type
Intervention
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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