Side Specific Withdrawal Times for Colonoscopy: Impact on Adenoma Detection in the Proximal and Distal Colon
NCT ID: NCT02819492
Last Updated: 2017-04-11
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
500 participants
OBSERVATIONAL
2014-11-30
2017-04-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Routine colonoscopy Cohort
Patients receiving routine colonoscopy at the study site
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* age ≥ 40 years
Exclusion Criteria
* pregnant women
* indication for colonoscopy: inflammatory bowel disease
* indication for colonoscopy: polyposis syndrome
* indication for colonoscopy: emergency colonoscopy e.g. acute bleeding
* contraindication for polyp resection e.g. patients on warfarin
40 Years
90 Years
ALL
No
Sponsors
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Technical University of Munich
OTHER
Responsible Party
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Locations
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II Medizinische Klinik am Klinikum rechts der Isar der Technischen Universität München
Munich, , Germany
Countries
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Other Identifiers
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SNOWCAT
Identifier Type: -
Identifier Source: org_study_id
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