Clinical Trials Directory

Trials / Completed

CompletedNCT01559727

Dose-comparison Study of Prednisone in Heart Failure

Randomized Dose-comparison Study of Prednisone in Patients With Symptomatic Heart Failure

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
40 (actual)
Sponsor
Hebei Medical University · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to examine the efficacy of three doses of prednisone, a glucocorticoid, in treatment of patients with symptomatic heart failure.

Detailed description

Heart failure is a leading cause of cardiovascular morbidity and mortality in the world. Most patients with acute symptomatic heart failure are admitted with fluid overload. Intravenous loop diuretics are an essential component of current treatment in such patients. Newly emerging evidence showed that glucocorticoids could potentiate natriuretic peptides' action by upregulating the expression natriuretic peptide receptor A (NPR-A) in the kidney, and produce a potent diuresis. Therefore, the investigators designed this nonblinded, randomized dose comparison study to compare the efficacy of prednisone at 15, 30 and 60 mg/day in patients with in symptomatic heart failure.

Conditions

Interventions

TypeNameDescription
DRUGprednisoneThe patients with symptomatic heart failure are treated with prednisone at dose of 15 mg/day.
DRUGprednisoneThe patients with symptomatic heart failure are treated with prednisone at dose of 30 mg/day
DRUGprednisoneThe patients with symptomatic heart failure are treated with prednisone at dose of 60 mg/day

Timeline

Start date
2012-03-01
Primary completion
2013-01-01
Completion
2013-03-01
First posted
2012-03-21
Last updated
2013-08-28

Locations

2 sites across 1 country: China

Source: ClinicalTrials.gov record NCT01559727. Inclusion in this directory is not an endorsement.