Diuretic and Renal Effects of Vaprisol When Administered Along With Furosemide and Nesiritide Continuous Infusion
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|ClinicalTrials.gov Identifier: NCT00806910|
Recruitment Status : Withdrawn (Sponsor support withdrawn)
First Posted : December 11, 2008
Last Update Posted : June 23, 2011
|Condition or disease||Intervention/treatment||Phase|
|Heart Failure||Drug: Conivaptan Other: Placebo||Phase 4|
Heart failure effects 5 to 6 million Americans and is increasing in prevalence. There are about 550, 000 new cases of heart failure every year and about 3 million admissions for acute decompensated heart failure every year. The total cost of heat failure on the health systems is upwards of 35 billion dollars per year. Despite advances in medical care, the hospital readmission rate is 20% at one month and 50% at six months. This prevailing situation mandates further exploration of novel therapeutic targets to treat this complex disease.
Vasopressin levels are often elevated in patients with heart failure and LV dysfunction which is paradoxical and inappropriate. It has been hypothesized that high levels of circulating vasopressin may play an important role not only in the pathophysiology of the heart failure syndrome but also contribute to its disease progression.
Studies have shown that Conivaptan, a Vasopressin antagonist results in favorable changes in hemodynamics and urine output without affecting blood pressure or heart rate. No consensus has been reached for Conivaptan to be used as a sole agent in Acute Decompensated Heart Failure (ADHF) patients and IV loop diuretics and/or vasodilators such as Nesiritide are used as the prime treatment for vascular congestion. This prevailing situation brings the questions whether, Conivaptan can be used as an adjunct to IV Furosemide and/or Nesiritide presenting with ADHF.We intend to investigate this question in a cohort of heart failure patients with hyponatremia.
This study will enroll 60 patients ( who meets all the inclusion criteria and none of the exclusion criteria), admitted to the Albert Einstein Medical Center with the diagnosis of Acute Decompensated Heart Failure (New York Heart Association class 3 and 4). The study population will be divided into 2 groups; a treatment group and a placebo group as described below. Each group will be comprised of 30 patients.
The treatment group will be treated with Nesiritide infusion, intravenous Furosemide (either continuous infusion or bolus injection- total dose of Furosemide received at the end of the study will be calculated) and IV Vaprisol. The placebo group will be given Nesiritide infusion and intravenous Furosemide(either continuous infusion or bolus injection) and placebo. Treatment will be continued in both groups for 24-36 hours.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||0 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)|
|Official Title:||Evaluation of the Diuretic and Renal Effects of Vaprisol When Administered Along With Furosemide and Nesiritide Continuous Infusion|
|Study Start Date :||October 2008|
|Primary Completion Date :||February 2010|
|Study Completion Date :||February 2010|
Active Comparator: Treatment
Subjects will be treated with Intravenous Vaprisol along with Nesiritide infusion and intravenous Furosemide (either continuous infusion or bolus injections - total dose of Furosemide received will be calculated at the end of the study).
IV Vaprisol initially at 20 mg IV injection over 30 minutes, followed by a 20 mg IV infusion over the next 24 hours (i.e. 20 mg bolus, 20 mg continuous infusion approximately 24 hrs).
Other Name: Vaprisol
Placebo Comparator: Placebo
Subjects will be given Placebo (at the same rate of Vaprisol given in the treatment arm) along with Nesiritide infusion and intravenous Furosemide (either continuous infusion or bolus injections - total dose of Furosemide received will be calculated at the end of the study).
Placebo (will be given at the same rate of Vaprisol given in the treatment arm)
Other Name: Saline
- Degree of diuresis as measured by weight change and intake and output measurement [ Time Frame: Post infusion, Pre discharge and at 30 day Post discharge ]
- Length of stay (LOS) in hospital [ Time Frame: Concurrent ]
- Clinical status based on NYHA criteria [ Time Frame: Pre-discharge and 30-day post-discharge follow up ]
- Serum electrolytes [ Time Frame: Pre and Post infusion ]
- BUN and Serum Creatinine concentration [ Time Frame: Post infusion, Pre discharge and at 30 day Post discharge ]
- Number of readmissions due to ADHF [ Time Frame: Within 30-day post-discharge follow up ]
- Dyspnea assessment by Visual Analog Scale score [ Time Frame: Post infusion, Pre discharge and at 30 day Post discharge ]
- Subjective feeling based on Minnesota - Living with Heart Failure Questionnaire [ Time Frame: Pre-discharge and 30-day post-discharge follow up ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00806910
|Principal Investigator:||Darshak H Karia, MD||Albert Einstein Medical Center|