RecruitingNCT06781242

Genotype-phenotype Relationship Between Cryptogenic Cholestasis and Familial Intrahepatic Cholestasis

Genotype-phenotype Relationship Between Adult Cryptogenic Cholestasis and Mutations in Genes Responsible for Progressive Familial Intrahepatic Cholestasis


Sponsor

IRCCS Azienda Ospedaliero-Universitaria di Bologna

Enrollment

300 participants

Start Date

Jan 16, 2024

Study Type

OBSERVATIONAL

Conditions

Summary

Genotype-phenotype relationship between adult cryptogenic cholestasis and mutations in genes responsible for progressive familial intrahepatic cholestasis


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is investigating a group of rare inherited liver conditions that cause bile to build up abnormally (cholestasis). Researchers want to better understand how genetic mutations lead to different symptoms and disease patterns in patients. **You may be eligible if...** - You are 18 or older - You have been diagnosed with PFIC (progressive familial intrahepatic cholestasis) or a related inherited liver condition causing bile flow problems - You are able to provide informed consent **You may NOT be eligible if...** - You have another documented cause of chronic liver disease that better explains your symptoms Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Locations(2)

IRCCS - Azienda Ospedaliero-Universitaria di Bologna

Bologna, Bologna, Italy

Ospedale Civile Sant'Agostino Estense Baggiovara

Modena, Modena, Italy

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NCT06781242


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