The purpose of the study is to investigate the efficacy and safety for the management of hyponatremia and ascites in patients with liver cirrhosis.
Patients with advanced cirrhosis frequently develop dilutional hyponatremia due to impairment of their renal ability to eliminate solute-free water. Although the pathophysiology of this disorder is multifactorial, an increased hypersecretion of arginine vasopressin (AVP) is a major factor. The prevalence of hyponatremia in cirrhosis, as defined by a serum sodium level of 130 mmol/L is reported to be about 20%, and there are several lines of evidence that hyponatremia is a risk factor for the development of hepatic encephalopathy, and that it predicts a poor quality of life independent of liver function. Hyponatremia also predicts short-term mortality in cirrhotic patients awaiting liver transplantation. The principle of the management of hypervolemic hypona- tremia is to induce a negative water balance, with the aim of normalizing the increased total body water, which would result in an improvement in serum sodium concentration. Fluid restriction is the most widely accepted nonpharmacological therapy, but its efficacy is very limited. The administration of hypertonic sodium chloride has been common in severe hypervolemic hyponatremia, but its effect is only partial and short lived; moreover, additional expansion of fluid can worsen ascites and edema. Therefore, the pathophysiologically oriented treatment of hyponatremia focuses on inhibiting the actions of AVP. Recently, antagonists of the V2 receptors of vasopressin has been proposed to manage hyponatremic patients, such as heart fauilure, syndrome of inappropriate antidiuretic hormone or liver cirrhosis. Especially, a lot of hyponatremic patients with cirrhosis had ascites, and some of them had intractable ascites. In these patients, antagonists of the V2 receptors of vasopressin including tolvaptan might have beneficial effect in enhancing not only hyponatremia , but also ascites
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
105
Konkuk University Medical Center
Seoul, Seoul, South Korea
the change in the average daily area under the curve (AUC) for the serum sodium concentration from baseline to day 28 after intervention
Time frame: baseline and 28 days
the change in the average daily area under the curve (AUC) for the serum sodium concentration from baseline to day 4
Time frame: baseline and 4 days
the time to normalization of the serum sodium concentration
Time frame: up to 28 days
the time to first paracentesis, number of paracentesis, the volume of ascitic fluid obtained from paracentesis
Time frame: up to 28 days
Abdominal discomfort based on a 100-mm visual analogue scales (VAS)
Time frame: day 1, 2, 3, 4, 7, 14, 21, 28
The change in the dose of concomitant diuretics from baseline at day 28
Time frame: day 1, 2, 3, 4, 7, 14, 21, 28
the number of participants with serious adverse events
Time frame: from baseline to day 28 after intervention
the time to ascites improvement
Time frame: up to 28 days
the time of worsening of ascites
Time frame: up to 28 days
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