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
| Type | Name | Description |
|---|---|---|
| DRUG | Nesiritide | Nesiritide: 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.