Expired Study
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New York, New York 10032


Purpose:

Low sodium levels (hyponatremia) are a frequent occurrence in medically ill patients, and in particular those with neurological injury. Hyponatremia has been associated with worse outcome, problems with memory and concentration and impaired balance. Standard treatment for low sodium (salt) levels is to give the patient a salt containing solution thru a catheter (small flexible tube) in a vein in the arm or leg. One of the major complications of this treatment is excess body fluid which may cause heart problems or accumulation of fluid in the lungs and may require additional medications to remove extra water from the body. FDA approval has recently been granted for a new drug - Conivaptan - for use in hyponatremic conditions. Conivaptan works by excreting free water from the body and thereby produce concurrent rise in serum sodium concentrations. Conivaptan has not been evaluated specifically in patients with brain injuries. The primary objective of this study is to demonstrate the safety and efficacy of intravenous Conivaptan for the treatment of hyponatremia in patients with brain injury. If effective, Conivaptan may represent a safe treatment option.


Criteria:

Inclusion Criteria: - Acute neurological injury - Euvolemia or hypervolemia (defined clinically by examination, recent I+Os, BUN/creatinine ratio and CVP [if available]) - Serum sodium less than or equal to 132 mEq/L (confirmed as hypoosmolar hyponatremia by a concurrent source: osmolality measurements [<280 mosoms/L] or by a preceding serum Na+ value <135 mEq/L0 Exclusion Criteria: - Patients who have uncontrolled hypertension; significant orthostatic hypotension or supine systolic blood pressure less than 85 mm Hg; - Uncontrolled arrhythmias; - Untreated severe hypothyroidism, hyperthyroidism, or adrenal insufficiency; - Estimated creatinine clearance less than 20 ml/min; - Urinary outflow obstruction unless catheterized; - Alanine aminotransferase (ALT) >3x ULN - Aspartate aminotransferase (AST) >3x ULN - Serum albumin of 1.5 g/dl or less; - Prothrombin time greater than 22 sec or an international normalized ratio (INR) greater than 2.0 without anticoagulant therapy or 3.0 or more with therapy; a white blood cell count less than 3000/µl; - HIV infection; - Active hepatitis. - Pregnant or nursing - Participation in a clinical trial of an investigational drug or device within 30 days of screening - Unable to obtain written consent


NCT ID:

NCT00684164


Primary Contact:

Principal Investigator
Stephan A. Mayer, MD
Columbia University


Backup Contact:

N/A


Location Contact:

New York, New York 10032
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: March 16, 2018

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