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Phase I Study of Colchicine Therapy in Childhood Hepatic Cirrhosis

N

National Center for Research Resources (NCRR)

Status and phase

Unknown
Phase 1

Conditions

Cirrhosis
Liver Cirrhosis

Treatments

Drug: colchicine

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT00004368
CHD-1089
199/11947

Details and patient eligibility

About

OBJECTIVES:

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

Full 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.

Sex

All

Ages

Under 17 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

  • Advanced hepatic fibrosis or cirrhosis in children
  • Not pregnant

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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