Tolvaptan for In-hospital Hyponatremia

NCT ID: NCT01386372

Last Updated: 2016-12-15

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE2
• Total Enrollment: 3 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2011-06-30
• Study Completion Date: 2012-11-30

Brief Summary

Hyponatremia is a common electrolyte disorder encountered in hospitalized patients. A preliminary, observational, feasibility analysis finalized to assess retrospectively the incidence of hyponatremia (Serum sodium < 135 mEq/L) in a general medical-surgical hospital and the distribution of the cases of hyponatremia among different referral units showed that over one year observation there were more than 1500 cases of hyponatremia. Conventional therapy for hyponatremia depends on its causes, speed of onset, extracellular fluid volume status, and severity. Treatment consists in fluid restriction, normal or hypertonic saline, furosemide. Recent development of arginine vasopressin antagonists has provided a new therapeutic option for treatment of hyponatremia.Tolvaptan, an orally administered, nonpeptide, selective vasopressin V2 receptor antagonist reported to increase free water clearance and limit fluid retention in subjects with congestive heart failure or liver cirrhosis, has been also shown to be effective in the treatment of chronic hyponatremia in patients with SIADH, chronic heart failure, liver cirrhosis. Thus the investigators designed a clinical study to explore the incidence of severe hyponatremia in hospitalized patients in the setting of large general hospital and to evaluate whether tolvaptan is effective and safe in increasing serum sodium concentration in patients with normovolemic and hypervolemic hyponatremia in the setting of daily clinical practice. Moreover this study may help understand the cost-effectiveness of tolvaptan therapy compared to traditional treatments of hyponatremia.

Conditions

Hyponatremia

Keywords

Hyponatremia; Vasopressin; Tolvaptan; SIADH

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Tolvaptan

Group Type: EXPERIMENTAL

Tolvaptan

Intervention Type: DRUG

Patients will receive full-dose oral tolvaptan therapy up to 1 month after randomization. During the initial 4 days of therapy, the dose of the study drug will be increased from 15 to 30 mg or from 30 to 60 mg according to a regimen designed for slow correction of serum sodium concentrations to 135 mEq/L or more Depending on the serum sodium concentration the dose will be increased or decreased. Patients will then be continued on their maintenance therapy with adjustments allowed to prevent hyponatremia and avoiding hypernatremia. As soon as normal serum sodium levels are achieved in at least two consecutive measurements the dose of the study drug will be progressively tapered according to an individually tailored weaning program

standard therapy

Group Type: ACTIVE_COMPARATOR

Standard therapy

Intervention Type: OTHER

Fluid restriction, normal or hypertonic saline, furosemide.

Interventions

Tolvaptan

Patients will receive full-dose oral tolvaptan therapy up to 1 month after randomization. During the initial 4 days of therapy, the dose of the study drug will be increased from 15 to 30 mg or from 30 to 60 mg according to a regimen designed for slow correction of serum sodium concentrations to 135 mEq/L or more Depending on the serum sodium concentration the dose will be increased or decreased. Patients will then be continued on their maintenance therapy with adjustments allowed to prevent hyponatremia and avoiding hypernatremia. As soon as normal serum sodium levels are achieved in at least two consecutive measurements the dose of the study drug will be progressively tapered according to an individually tailored weaning program

Intervention Type: DRUG

Standard therapy

Fluid restriction, normal or hypertonic saline, furosemide.

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Non artifactual hyponatremia in euvolemic or hypervolemic states, defined as serum sodium <135 mEq/L confirmed in at least 2 consecutive evaluations;
• 18 years of age or older;
• Able to give written Informed Consent.

Exclusion Criteria

• Women who are breast feeding and females of childbearing potential who are not using acceptable contraceptive methods;
• Hyponatremia in hypovolemic states;
• Acute and transient hyponatremia associated with head trauma or post-operative state;
• Hyponatremia due to uncontrolled hypothyroidism or uncontrolled adrenal insufficiency;
• Cardiac surgery within 30 days prior to the potential study enrollment, excluding percutaneous coronary interventions;
• History of a myocardial infarction within 30 days prior to the potential study enrollment;
• History of sustained ventricular tachycardia or ventricular fibrillation within the last 30 days, unless in the presence of an automatic implantable cardioverter defibrillator;
• Severe angina including angina at rest or at slight exertion and/or unstable angina;
• History of a cerebrovascular accident within the last 30 days;
• Subjects with psychogenic polydipsia may not be included, however subjects with other psychiatric illness may be included;
• Systolic arterial blood pressure <90 mmHg;
• History of hypersensitivity and/or idiosyncratic reaction to benzazepine or benzazepine derivatives (such as benazepril);
• History of drug or medication abuse within the past year, or current alcohol abuse;
• Uncontrolled diabetes mellitus defined as fasting glucose >300mg/dL;
• Urinary tract obstruction except BPH if non-obstructive;
• Terminally ill or moribund condition with little chance of short-term survival;
• Serum creatinine >3.5 mg/dL;
• Serum sodium <120 mEq/L with associated neurologic impairment, i.e. symptoms such as apathy, confusion, seizures;
• Patients with progressive or episodic neurologic disease such as multiple sclerosis or history of multiple strokes;
• Child-Pugh score greater than 10 (unless approved);
• Patients receiving intravenous fluids at a rate greater than KVO (Keep Vein Open);
• Hyponatremia due to lab artifacts;
• Patients receiving AVP or its analogs for treatment of any condition;
• Patients receiving within 7 days of randomization, other medications for treatment of hyponatremia specifically: demeclocycline, lithium carbonate or urea;
• Patients likely requiring IV saline for correction of symptomatic or asymptomatic severe hyponatremia during the course of the study;
• Severe pulmonary artery hypertension;
• Hyponatremia should not be the result of any medication that can safely be withdrawn.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

A.O. Ospedale Papa Giovanni XXIII

OTHER

Sponsor Role: collaborator

Mario Negri Institute for Pharmacological Research

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

OO.RR., Bergamo - Unit of Nephrology and Dialisis

Bergamo, , Italy

Countries

Italy

Other Identifiers

2010-024431-17

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

INSERT

Identifier Type: -

Identifier Source: org_study_id