- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01039272
Epstein-Barr Detection in Oral Cancer
June 24, 2015 updated by: UPECLIN HC FM Botucatu Unesp
Epstein-Barr Detection in Squamous Cell Carcinoma and Healthy Oral Mucosa
The aim of this study is to analyze oral squamous cell carcinoma and healthy oral mucosa for the possible presence of Epstein-Barr virus (EBV).
Study Overview
Status
Completed
Conditions
Detailed Description
Epstein-Barr virus has been implicated in a range of malignant neoplasms, including in some studies, in the aetiology of oral squamous cell carcinoma but the influence of EBV in oral cancer remains unclear.
This study will examine the prevalence of EBV infection in oral cancer by means of nested polymerase chain reaction.
Study Type
Observational
Enrollment (Actual)
60
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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São Paulo
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Araçatuba, São Paulo, Brazil, 16025-050
- Department of Pathology and Propaedeutics, Sao Paulo State University, Unesp, Araçatuba/SP
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
40 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
oral care clinic, community sample
Description
Inclusion Criteria:
- patients of Oral Cancer Centre - UNESP/Araçatuba - SP
- with oral squamous cell carcinoma
Exclusion Criteria:
- without oral squamous cell carcinoma
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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oral cancer
patients with oral squamous cell carcinoma
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control group
healthy patients without any oral pathology
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
presence of EBV
Time Frame: 1 hour
|
Epstein-Barr virus has been implicated in a range of malignant neoplasms, including in some studies, in the aetiology of oral squamous cell carcinoma but the influence of EBV in oral cancer remains unclear.
This study will examine the prevalence of EBV infection in oral cancer by means of nested polymerase chain reaction.
|
1 hour
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Glauco Issamu I Miyahara, Professor, Department of Pathology and Propaedeutics, Sao Paulo State University, Unesp, Araçatuba/SP
- Study Chair: Lívia T Arêde, student, Department of Pathology and Propaedeutics, Sao Paulo State University, Unesp, Araçatuba/SP
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
March 1, 2008
Primary Completion (Actual)
April 1, 2008
Study Completion (Actual)
June 1, 2015
Study Registration Dates
First Submitted
December 22, 2009
First Submitted That Met QC Criteria
December 22, 2009
First Posted (Estimate)
December 24, 2009
Study Record Updates
Last Update Posted (Estimate)
June 25, 2015
Last Update Submitted That Met QC Criteria
June 24, 2015
Last Verified
June 1, 2015
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- upeclin/FOA-Unesp-03
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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