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Intravenous Interferon During Liver Transplant

Wake Forest University (WFU) logo

Wake Forest University (WFU)

Status

Completed

Conditions

Cirrhosis
Hepatitis C

Treatments

Drug: IV interferon

Study type

Interventional

Funder types

Other

Identifiers

NCT01192698
04-05-09A

Details and patient eligibility

About

The main goal of this study is to prevent liver allograft infection with Hepatitis C virus in hepatitis C positive patients undergoing liver transplantation. The hypothesis is that patients who receive ribavirin immediately before transplant and intravenous interferon alfa 2b during the anhepatic phase(while the liver is removed)will have sustained virologic response post liver transplant.

Full description

The study is evaluating intravenous interferon given during the anhepatic phase of lvier transplant. Ribavirin was given as well. Serial measurements for HCV RNA were determined 12, 24 72, 96 hrs and 4 weeks after liver transplant.

Enrollment

15 patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • liver transplant for hepatitis c

Exclusion criteria

  • allergy to interferon

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

15 participants in 2 patient groups

IV interferon
Experimental group
Description:
IV interferon oral ribavirin
Treatment:
Drug: IV interferon
Standard of care
No Intervention group
Description:
standard of care

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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