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NCT00341484 · ClinicalTrials.gov registry record

Genetic Susceptibility to Oncogenic Viruses

A clinical trial, sponsored by National Cancer Institute (NCI).

Completed
Registry status
2,580
Enrollment target

NCT00341484: Completed study, sponsored by National Cancer Institute (NCI).

NCT00341484 is a clinical trial that has completed, run by National Cancer Institute (NCI). The registered enrollment target is 2,580 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00341484 has completed, sponsored by National Cancer Institute (NCI).

COMPLETED
Registry status
2,580 participants
Enrollment target

Study Summary

An NCI goal is to identify every human gene that predisposes people to cancer. Recent studies of HIV-1 indicate that genetic polymorphisms can affect susceptibility to viral infections and that such alleles may be racially restricted, a range of racial and ethnic groups should be included in such studies. We propose to examine genetic determinants of infection with hepatitis B virus (HBV) and hepatitis C virus (HCV) in an ethnically diverse population of injection drug users (IDUs). HBV and HCV are important causes of hepatocellular carcinoma, but little is known about genetic factors that alter susceptibility to these infections. Subjects will be recruited in diverse inner-city neighborhoods as part of the University of California, San Francisco's Urban Health Study. Since 1986, this study has successfully recruited and evaluated IDUs from street-based settings. About half of the participants are African-American, one-third are white, 10% are Latino, and the remainder are Asian or Native American. The mean duration of drug use exceeds 20 years. About 80% of subjects have evidence of HBV infection and a similar prevalence of HCV infections is anticipated. We will enroll about 1500 subjects over a 13 month period. Archived, unlinked serum specimens may be obtained from previous enrollees to increase the sample size, as needed. Highly exposed-uninfected subjects will be ascertained on the basis of the serologic testing for each virus, as well as the duration and frequency of injection drug use. These highly exposed-uninfected subjects will be compared to infected subjects with regard to their frequency of genetic polymorphisms (chemokines, chemokine receptors, human leukocyte antigens, and others), in collaboration with scientists from NCI's Laboratory of Genomic Diversity.

Primary Outcome

genetic determinants

Trial Details

FieldValue
Enrollment Target 2,580 participants
Start Date 1998-06-01
Est. Completion 2007-06-05
National Cancer Institute (NCI)

3,257 total trials

What the finished NCT00341484 record still lists

NCT00341484 is an observational study that tracks outcomes without assigning an intervention. Its 2,580 participants enrollment target places it among the larger protocols in the corpus.

The record links to 0 conditions, and to 0 interventions.

NCT00341484 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00341484 about?

NCT00341484 is a clinical study titled "Genetic Susceptibility to Oncogenic Viruses". An NCI goal is to identify every human gene that predisposes people to cancer. Recent studies of HIV-1 indicate that genetic polymorphisms can affect susceptibility to viral infections and that such alleles may be racially restricted, a range of racial and ethnic groups should be included in such st...

What is the current status of trial NCT00341484?

This trial is currently completed. The enrollment target is 2,580 participants. The study started on 1998-06-01. Estimated completion is 2007-06-05.

Who is sponsoring clinical trial NCT00341484?

This trial is sponsored by National Cancer Institute (NCI), which has 3,257 total clinical trials registered on ClinicalTrials.gov.

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Source: ClinicalTrials.gov NCT00341484, the US trial registry maintained by the National Library of Medicine. NCT00341484 (large enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.