Anemia in Heart Failure With a Preserved Ejection Fraction (HFPEF)

PHASE2CompletedINTERVENTIONAL
Enrollment

56

Participants

Timeline

Start Date

July 31, 2007

Primary Completion Date

November 30, 2012

Study Completion Date

November 30, 2012

Conditions
Anemia
Interventions
DRUG

Erythropoietin alpha

Erythropoietin alpha is administered weekly by subcutaneous injection using a pre-specified dosing algorithm. The dosing algorithm is designed to make adjustments based on the rate of rise (ROR) of the hemoglobin over a one week period, as well as the absolute hemoglobin value. Subjects initially received active treatment with 7,500 units of erythropoietin given weekly by subcutaneously injection. Subjects are carefully monitored (e.g. every week) to avoid rapid increases in hemoglobin/hematocrit and/or increasing blood pressure control. Dose adjustments are made if the hemoglobin rises too rapidly (greater than 0.3 g/dL) in any given weekly interval.

DRUG

Placebo

Placebo

Trial Locations (1)

10034

Clinical Cardiovascular Research Laboratory for the Elderly, New York

All Listed Sponsors
collaborator

National Institute on Aging (NIA)

NIH

lead

Mathew S. Maurer

OTHER

NCT00286182 - Anemia in Heart Failure With a Preserved Ejection Fraction (HFPEF) | Biotech Hunter | Biotech Hunter