drugset / Trial / NCT00372762

Bumetanide Versus Furosemide in Heart Failure

NCT00372762

RandomizedCrossoverQuadruple-blindTreatment

Summary

Patients with NYHA FC II-III heart failure will be randomized in a cross-over fashion to 8 weeks of bumetanide versus furosemide therapy (equipotent dose), to test whether bumetanide therapy has a superior effect on insulin resistance compared to furosemide. Patients will be subject to a frequently sampled intravenous glucose tolerance test (FSIGT) with minimal model (MINMOD) analysis to assess insulin resistance and to a 6-minute walk test (6MWT) to assess functional capacity; patient recruitment and retention success, as well as medication adherence, will also be assessed.

Timeline

Start
2011-01
Primary completion
2013-01
Completion
2013-06

Drugs

EvaluationDrugModalityDoseRoute
Comparator Bumetanide Small molecule 0.5 mg Oral
Comparator Bumetanide Small molecule 2 mg Oral
Comparator Furosemide Other / unclassified 20 mg Oral
Comparator Furosemide Other / unclassified 80 mg Oral

Indications