Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
500 participants
INTERVENTIONAL
2012-04-30
2016-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
PREVENTION
NONE
Study Groups
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HPV detection in anal canal samples
HPV detection in anal canal samples
Additional anal taking during the colonoscopy with cytobrush
Interventions
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HPV detection in anal canal samples
Additional anal taking during the colonoscopy with cytobrush
Eligibility Criteria
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Inclusion Criteria
* patients undergoing colonoscopy under general anesthesia for any purpose
* signed written consent
Exclusion Criteria
* Absence of written consent.
* patients incapable of giving consent
18 Years
ALL
No
Sponsors
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Centre Hospitalier Universitaire de Besancon
OTHER
Responsible Party
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Locations
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Centre Hospitalier Régional Universitaire de Besançon
Besançon, , France
Centre Hospitalier Intercommunal de la Haute Saône
Vesoul, , France
Countries
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Other Identifiers
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API/2012/34
Identifier Type: -
Identifier Source: org_study_id
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