drugset / Trial / NCT00372762
Bumetanide Versus Furosemide in Heart Failure
Phase 3
Withdrawn
London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
University of Western Ontario, Canada · collab
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |