This study is being done to evaluate the safety and effectiveness of alagebrium in subjects diagnosed with diastolic heart failure. The primary assessment for effectiveness is the assessment of exercise tolerance.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
160
200 mg (two 100 mg tablets) two times daily for 24 weeks
placebo tablets - two tablets taken twice daily
Unnamed facility
Birmingham, Alabama, United States
The primary efficacy measure will be exercise tolerance as assessed utilizing the 6 Minute Walk Test
Time frame: Assessed at baseline, week 12 and week 24
QOL as assessed by the Kansas City Cardiomyopathy Questionnaire
Time frame: baseline, week 12 and week 24
To assess New York Heart Association Classification
Time frame: Baseline, week 12 and week 24
To evaluate cardiovascular death or hospitalization for heart failure
Time frame: Will be assessed during the entire 24 wk trial
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Unnamed facility
Huntsville, Alabama, United States
Unnamed facility
Mobile, Alabama, United States
Unnamed facility
Anaheim, California, United States
Unnamed facility
Bakersfield, California, United States
Unnamed facility
La Jolla, California, United States
Unnamed facility
Roseville, California, United States
Unnamed facility
Jacksonville, Florida, United States
Unnamed facility
Miami, Florida, United States
Unnamed facility
St. Petersburg, Florida, United States
...and 20 more locations