Clinical Trials Directory

Trials / Completed

CompletedNCT00982423

The Effects of Decreasing the Lasix Dose on the Cardiorenal System

To Define the Effects of Decreasing the Furosemide Dose on Cardiorenal and Humoral Function in Humans With Compensated Chronic Heart Failure (CHF) With and Without Renal Dysfunction

Status
Completed
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
41 (actual)
Sponsor
Mayo Clinic · Academic / Other
Sex
All
Age
18 Years – 90 Years
Healthy volunteers
Not accepted

Summary

The investigators' objective is to define the effects of decreasing the furosemide dose on heart, kidney and humoral function in people with compensated heart failure and kidney dysfunction and also in people with compensated heart failure without kidney dysfunction. Secondly, to define the humoral activation in both groups.

Detailed description

The broad objective of this protocol is to advance our understanding of the pathophysiological mechanisms of human Cardiorenal Syndrome (CRS) with a specific emphasis upon the biological interaction between diuretic therapy, the renin-angiotensin-aldosterone-system (RAAS) and cyclic 3'-5'-guanosine monophosphate (cGMP) pathway.

Conditions

Interventions

TypeNameDescription
DRUGFurosemideSubjects received their clinically prescribed dose of furosemide for a 3 week stabilization period, then were assessed for cardiorenal and humoral function. Subjects then had a 50% reduction of the furosemide dose for a 3 week stabilization period, and were assessed for cardiorenal and humoral function again.

Timeline

Start date
2009-07-01
Primary completion
2014-07-01
Completion
2014-07-01
First posted
2009-09-23
Last updated
2015-07-20
Results posted
2015-07-20

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00982423. Inclusion in this directory is not an endorsement.