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Comparison between the effects of spironolactone and eplerenone in the treatment of heart failure

Phase 3
Recruiting
Conditions
Systolic heart failure.
Left ventricular failure
I50.1
Registration Number
IRCT20130422013090N4
Lead Sponsor
Sari University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
70
Inclusion Criteria

New onset symptomatic systolic heart failure with left ventricular systolic ejection fraction less than 40%

Exclusion Criteria

Pregnancy
Previous use of aldosterone antagonists
Severe coronary artery disease with need to revascularization

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
eft ventricular ejection fraction. Timepoint: at the beginning of the study and 6 months after starting treatment. Method of measurement: Echocardiography.;Global longitudinal systolic strain. Timepoint: at the beginning of the study and 6 months after starting treatment. Method of measurement: Echocardiography.
Secondary Outcome Measures
NameTimeMethod
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