Clinical Trials Directory

Trials / Completed

CompletedNCT00119691

Nesiritide Infusion for the Treatment of Decompensated Heart Failure and Renal Dysfunction

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
34 (actual)
Sponsor
Brigham and Women's Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The researchers hypothesize that the addition of nesiritide to standard therapy will prevent worsening of renal function in patients admitted to the hospital with decompensated heart failure and renal dysfunction relative to standard therapy alone.

Conditions

Interventions

TypeNameDescription
DRUGNesiritideNesiritide: 1 mcg/kg bolus, followed by a continuous infusion at 0.005 mcg/kg/min which can be titrated every 3 hours by 0.005 mcg/kg/min to maximum dose of 0.03 mcg/kg/min until adequate diuresis achieved.

Timeline

Start date
2003-04-01
Primary completion
2005-11-01
Completion
2005-11-01
First posted
2005-07-14
Last updated
2013-09-12

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00119691. Inclusion in this directory is not an endorsement.