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
| Type | Name | Description |
|---|---|---|
| DRUG | Furosemide | Subjects 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.