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OpenTrials
Completed

NCT Number: NCT01192698

Intravenous Interferon During Liver Transplant

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.

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Key information

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • liver transplant for hepatitis c

Exclusion criteria

  • allergy to interferon

Treatment and study plan

IV interferon

Drug

IV interferon 5MU during anhepatic phase

Primary outcomes

  1. HCV RNA Result

    Time frame: 4 weeks after liver transplant

    Will measure mean HCV RNA levels 4 weeks after liver transplant

Sponsors and collaborators

Lead sponsor

Wake Forest University Health Sciences

Other

Collaborators

  • American College of Gastroenterology

Registry information

Official study title

Intravenous Interferon During the Anhepatic Phase of Liver Transplantation and Prevention of Recurrence of Hepatitis C Virus

Important dates

Study start
2009
Primary completion
2013
Study completion
2013
First posted
Sep 1, 2010
Registry last updated
Apr 21, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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