drugset / Trial / NCT03709160

Oral dIuretics in Very Intensive Treatment, an Early Intervention in Outpatients With Heart Failure

NCT03709160

Phase 4 Unknown 40 enrolled Centro en Insuficiencia Cardiaca, Mexico
RandomizedParallel-groupOpen-labelTreatment

Summary

In the present study, consecutive patients, older than 18 years, of both genders will be included. The diagnosis of reduced Heart Failure (HfrEF) according to: Clinical pattern, laboratories and Cardiac imaging (ESC criteria). Treatment will be assigned in two groups: Bumetanide and another group will be received Indapamide. Each group received maximum tolerated dose for seven days with Clinical and labs evaluations will be every 48 hrs. (Face-to-face and/or telephone visits). Serum and urinary labs, EKG´s, Echo will be evaluated. Daily in-home register will made. Final points were: Mortality, Urinary failure, Clinical Impairment, Hospital admissions, Oedema. (MUCHO). All patients will be followed for 30 days.

Timeline

Start
2018-10-15
Primary completion
2019-10-15
Completion
2019-10-15

Drugs

EvaluationDrugModalityDoseRoute
Subject Bumetanide Small molecule 1 mg Oral