Phase I Study of Colchicine Therapy in Childhood Hepatic Cirrhosis

Status Active, not recruiting

Clinical Trial Summary

OBJECTIVES:

I. Investigate the efficacy and safety of colchicine therapy in improving hepatic function and reducing hepatic fibrosis (scarring) in children with hepatic cirrhosis.

Clinical Trial Description

PROTOCOL OUTLINE: Patients receive colchicine orally twice daily for 24 months. After the first month, the dose of colchicine will increase and remain at that dose for the duration of study.

Patients are evaluated every 6 months during study. ;

Study Design

Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00004368
Study type	Interventional
Source	Office of Rare Diseases (ORD)
Contact
Status	Active, not recruiting
Phase	Phase 1
Start date	May 1990

View Details

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