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An exploratory study of susceptible factors to tolvaptan treatment in hepatic edema

Not Applicable
Conditions
iver cirrhosis with refractory hepatic edema
Registration Number
JPRN-UMIN000017318
Lead Sponsor
Department of Gastroenterology and Hepatology, Tokai University School of Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
50
Inclusion Criteria

Not provided

Exclusion Criteria

1)Alcoholic hepatitis and cirrhosis patients in continued drinking 2)Patients with overt hepatic encephalopathy 3)Patients with requiring treatment for esophageal, gastric or rectal varices 4)Hepatocellular carcinoma with life expectancy less than 3 months 5)The anuria patints (including dialysis patients) 6)Patients with urinary excretion failure 7)Patients with oral intake difficulty 8)Patients receiving albumin within 7 days before the test 9)Patients with unsuitable condition for this study

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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