drugset / Trial / NCT00180674

Anticoagulation in Liver Fibrosis in Patients With Hepatitis C Virus Infection

NCT00180674

Phase 2 Completed 14 enrolled Imperial College London
NaSingle-groupOpen-labelTreatment

Summary

Patients who have been treated for hepatitis C virus (HCV) infection who have failed to respond to anti-viral treatment are often concerned about their ongoing liver disease and are therefore looking for alternative treatments which might prevent fibrosis progression. This view is endorsed by patient representative groups (including Charles Gore at the HepC Trust) who have welcomed this trial protocol. The study is a single centred, prospective, open labelled design. Practical as well as safety concerns dictated that the study could not be conducted in a blinded fashion, since patients taking anticoagulation require monitoring. The study consisted of two 8 week phases: Phase 1 and Phase 2. Phase 1 (observation phase, 0 to 8 weeks) and Phase 2 (treatment phase with warfarin anticoagulation, 8 to 16 weeks). Study completed at end of Phase 2.

Timeline

Start
2005-08
Primary completion
2006-09
Completion
2006-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Warfarin Small molecule