Longitudinal Study of Genetic Causes of Intrahepatic Cholestasis (LOGIC)

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Conditions studied: Liver Diseases, Alagille Syndrome, Alpha 1-Antitrypsin Deficiency

In brief

Cholestasis is a condition in which bile is not properly transported from the liver to the small intestine. Cholestasis can be caused by an array of childhood diseases, including the genetic diseases Alagille syndrome (ALGS), alpha-1 antitrypsin (a-1AT) deficiency, bile acid synthesis and metabolism defects, and progressive familial intrahepatic cholestasis (PFIC) or benign recurrent intrahepatic cholestasis(BRIC). This study will investigate the natural history and progression of the four previously mentioned cholestatic liver diseases to provide a better understanding of the causes and effects of the diseases.

Key facts

Study ID
NCT00571272
Run by
Arbor Research Collaborative for Health
People needed
1675
Starts
2007-11-30
Expected to finish
2029-05-31
Last updated by the study team
2026-06-04

Who can join

Age: any, up to 25. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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