ICD K83.0ORPHA:171PSC

Primary Sclerosing Cholangitis

Primary Sclerosing Cholangitis is a chronic progressive disease of the bile ducts characterised by inflammation and fibrosis, leading to strictures, liver failure, and a significantly elevated risk of cholangiocarcinoma. It is strongly associated with inflammatory bowel disease, particularly ulcerative colitis. No effective medical treatment exists; liver transplantation is the only definitive therapy for advanced disease.

605
Articles
118
Trials (5 AU)
Updated
5 April 2026
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Common Questions

What is Primary Sclerosing Cholangitis?

Primary Sclerosing Cholangitis is a chronic progressive disease of the bile ducts characterised by inflammation and fibrosis, leading to strictures, liver failure, and a significantly elevated risk of cholangiocarcinoma. It is strongly associated with inflammatory bowel disease, particularly ulcerative colitis. No effective medical treatment exists; liver transplantation is the only definitive therapy for advanced disease.

How many clinical trials are available for Primary Sclerosing Cholangitis?

RareWays currently indexes 118 clinical trials for Primary Sclerosing Cholangitis, of which 27 are actively recruiting. Trial availability changes as new studies are registered — check the trials tab for current status.

Where does the research data for Primary Sclerosing Cholangitis come from?

RareWays aggregates research from PubMed, Europe PMC, OpenAlex, and ClinicalTrials.gov. Data is updated regularly by Rocky, RareWays' automated research engine. All articles and trials link directly to their original sources.

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For guidance specific to your situation, please speak with your healthcare team.