drugset / Trial / NCT00125996

Effect of Intravenous Ferrous Sucrose on Exercise Capacity in Chronic Heart Failure

NCT00125996

RandomizedParallel-groupSingle-blindTreatment

Summary

This is a two-center, randomised, single-blind (physician), prospective, controlled study to assess the acute (8 weeks) and chronic (16 weeks) effects of intravenous (IV) iron sucrose supplementation in anaemic and non-anaemic iron deficient patients with chronic heart failure (CHF). The hypotheses are: * Treatment of anaemic and non-anaemic iron-deficient CHF patients with IV iron sucrose improves exercise capacity as measured by peak VO2. * IV iron sucrose is safe and well tolerated in subjects with moderate to severe CHF.

Timeline

Start
2004-07
Primary completion
Completion
2006-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Iron sucrose Unknown 200 mg Intravenous