Cholangitis, Sclerosing, Liver Cirrhosis, Biliary
Conditions
Keywords
cirrhosis, gastrointestinal disorders, primary biliary cirrhosis, primary sclerosing cholangitis, rare disease
Brief summary
OBJECTIVES: I. Assess the safety and effectiveness of budesonide in patients with primary sclerosing cholangitis or primary biliary cirrhosis experiencing a suboptimal response to ursodeoxycholic acid. II. Estimate the efficacy of this therapy in these patient groups as a means of evaluating the feasibility of a long-term randomized trial.
Detailed description
PROTOCOL OUTLINE: Patients receive budesonide by mouth 3 times daily for a minimum of 6 months. If liver biochemistries become normal, dosage is reduced to once daily. Treatment discontinues after 1 year.
Interventions
Oral budesonide, 9 mg daily was administered for 1 year
Sponsors
Study design
Eligibility
Inclusion criteria
PROTOCOL ENTRY CRITERIA: --Disease Characteristics-- Pathologically confirmed primary sclerosing cholangitis (PSC) meeting the following criteria: * Chronic cholestatic disease for at least 6 months * Liver biopsy within the past 6 months compatible with the diagnosis of PSC Intra and/or extrahepatic biliary duct obstruction, beading, or narrowing OR Pathologically confirmed primary biliary cirrhosis (PBC) that is experiencing suboptimal response to ursodeoxycholic acid and meeting the following criteria: * Chronic cholestatic liver disease for at least 6 months * Positive antimitochondrial antibody * No biliary obstruction by ultrasound, CT, or cholangiography * Prior liver biopsy compatible with diagnosis of PBC * Received ursodeoxycholic acid for at least 6 months --Prior/Concurrent Therapy-- Biologic therapy: * At least 3 months since prior D-penicillamine * No planned transplantation for at least 1 year Chemotherapy: * At least 3 months (6 months for PBC) since prior cyclosporin, colchicine, azathioprine, or methotrexate * At least 6 months since prior chlorambucil (PBC only) Endocrine therapy: At least 3 months (6 months for PBC) since prior corticosteroids Surgery: No prior intraductal stones or operations on the biliary tree except cholecystectomy (PSC only) Other: * At least 3 months since prior pentoxifylline, ursodeoxycholic acid, or nicotine (PSC only) * At least 6 months since prior chenodeoxycholic acid (PBC only) --Patient Characteristics-- Life expectancy: At least 3 years Hematopoietic: Not specified Hepatic: * Alkaline phosphatase at least 2 times upper limits of normal * No chronic hepatitis B infection * No hepatitis C infection * No autoimmune hepatitis * Bilirubin no greater than 4 mg/dL (PBC only) Cardiovascular: No severe cardiopulmonary disease Other: * No concurrent advanced malignancy * At least 3 months since prior inflammatory bowel disease requiring specific treatment except maintenance therapy (PSC only) * No anticipated need for transplantation within 1 year * Not pregnant * No liver disease of other etiology such as: Chronic alcoholic liver disease Hemochromatosis Wilson's disease Congenital biliary disease Cholangiocarcinoma No recurrent ascending cholangitis requiring hospitalization more than 2 times per year (PSC only) At least 1 year since prior active peptic ulcer No recurrent variceal bleeds No spontaneous encephalopathy No diuretic-resistant ascites
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in serum alkaline phosphatase | 1 year |
Countries
United States