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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00435201
Other study ID # ECH-0596
Secondary ID
Status Completed
Phase N/A
First received February 13, 2007
Last updated August 6, 2013
Start date January 2007
Est. completion date June 2013

Study information

Verified date August 2013
Source Rockefeller University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

The purpose of this study is to investigate the mechanism of autoantibody production during chronic hepatitis C virus (HCV) infection. 10-50% of individuals with HCV have symptoms of mixed cryoglobulinemia (MC). By studying the B cells from HCV-infected individuals with and without MC, as well as from healthy controls, we hope to gain insight into the mechanisms of autoantibody production and develop new strategies for treatment of MC.


Description:

Hepatitis C virus (HCV) infects approximately 170 million people worldwide. About 10-50% of persons with HCV have MC. MC is associated with the development of autoimmune symptoms and B cell proliferative disorders. We plan to study B cells from individuals chronically infected with HCV as well as from healthy controls. We sort B cells into different types, and we analyze these types for differential levels of gene expression. We are testing the hypothesis that certain types of B cells from subjects with MC have increased expression of genes that allow for increased cell survival.

People interested in participating in this study will have a complete history and general medical examinations before beginning the study. Following the screening, you will have a procedure called leukapheresis, in which white blood cells are removed, but your own red blood cells are returned. The procedure takes approximately 3 hours and is similar to blood donation. The leukapheresis is done during a same day admission to the hospital by an outside blood collection company with trained nurses and certified equipment.

Some aspects of this study are experimental which means the fluid and cells collected will be studied and analyzed to determine more precisely how your body's immune system is responding to the virus. These tests are experimental in that they are not part of the usual routine care of patients.


Recruitment information / eligibility

Status Completed
Enrollment 14
Est. completion date June 2013
Est. primary completion date June 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- At least 18 years of age.

- Ability to give informed consent.

- WBC greater than 3,000/mm3.

- Platelets greater than 80,000/mm3.

- Hb at least 9.5 g/dl.

- INR less than 1.5.

- Biologic therapy: Greater than 6 months post-Rituximab therapy.

- Greater than 6 months post IFN- alpha and Ribavirin therapy.

Exclusion Criteria:

- Decompensated cirrhosis.

- Serious uncontrolled medical illness.

- Receipt of immune modulators or suppressors within 30 days prior to study entry, including, but not limited to, interferons and thalidomide.

- Psychiatric illness or social condition that, in the opinion of the investigator, would interfere with adherence to study requirements.

- Alcohol or drug use or dependence that, in the opinion of the investigator,would interfere with adherence to study requirements.

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
United Kingdom Oxford University Oxford
United States Rockefeller University Hospital New York New York

Sponsors (2)

Lead Sponsor Collaborator
Rockefeller University New York Presbyterian Hospital

Countries where clinical trial is conducted

United States,  United Kingdom, 

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