Phase
Condition
Gall Bladder Disorders
Liver Disease
Liver Disorders
Treatment
N/AClinical Study ID
Ages 18-75 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Adult patients between 18 and 75 years of age (inclusive) who can comprehendinstructions, follow the study procedures and are willing to sign an InformedConsent Form (ICF).
Confirmed clinical diagnosis of large duct PSC based on current AASLD Guidelines (Bowlus 2023).
Exclusion
Exclusion Criteria:
Clinically significant acute or chronic liver disease of an etiology other than PSC (with or without presence of features of AIH).
Small-Duct PSC.
Clinically diagnosed secondary or IgG4-related sclerosing cholangitis.
Clinically diagnosed acute cholangitis and currently receiving treatment. Patientson chronic suppressive antibiotics will be allowed to enroll.
UDCA dose >28 mg/kg
Evidence of current or historical decompensated cirrhosis based on the followingclinical events:
Ascites > Grade 2 and requiring treatment
Esophageal or gastric variceal bleeding requiring hospitalization
Hepatic encephalopathy (as defined by a West Haven score ≥ 2)
Spontaneous bacterial peritonitis defined as ascites absolute neutrophil count >250/mm3 in the absence of an intra-abdominal source of infection
AKI-HRS according to AASLD Guidelines (Flamm 2021)
Prior liver transplantation
MELD-Na Score >15. For subjects on anticoagulation medication, baseline INRdetermination for MELD score calculation should take this use into account.
Participants with current clinical or laboratory evidence of any severe,progressive, or uncontrolled disease, related or unrelated to PSC and which, in theopinion of the investigator, has an expected survival of less than 48 weeks.
Participants who are impaired, incapacitated, or incapable of completing study-related assessments or giving informed consent.
Prisoners or participants who are involuntarily incarcerated.
Participants who are currently participating in an interventional clinical study.
Absence of data in medical records to assess inclusion and exclusion criteria.
Study Design
Study Description
Connect with a study center
University of Alberta
Edmonton, Alberta T6G 2X8
CanadaActive - Recruiting
University Health Network
Toronto, Ontario M5G2C4
CanadaActive - Recruiting
University Medical Center Hamburg-Eppendorf
Hamburg, 20246
GermanyActive - Recruiting
UC Davis
Sacramento, California 95817
United StatesActive - Recruiting
California Pacific Medical Center
San Francisco, California 94109
United StatesActive - Recruiting
University of California, San Francisco
San Francisco, California 94143
United StatesActive - Recruiting
Schiff Center for Liver Diseases / University of Miami
Miami, Florida 33136
United StatesActive - Recruiting
Indiana University
Indianapolis, Indiana 46202
United StatesActive - Recruiting
Massachusetts General Hospital
Boston, Massachusetts 02114
United StatesActive - Recruiting
Virginia Commonwealth University
Richmond, Virginia 23298
United StatesActive - Recruiting
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