The Role of the Fujinon Intelligent Chromo Endoscopy (FICE™) in Barrett's Esophagus
NCT ID: NCT01084629
Last Updated: 2021-12-15
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
50 participants
OBSERVATIONAL
2010-11-30
2016-11-04
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Surveillance Barrett's esophagus
Patients scheduled for endoscopic surveillance of Barrett's esophagus
No interventions assigned to this group
Barrett's esophagus post ablation
Patients scheduled for surveillance endoscopy who have undergone ablative therapies (PDT, RF ablation) for their Barrett's esophagus
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Scheduled for Surveillance Endoscopy
* Able to undergo endoscopy
Exclusion Criteria
* Unable to stop blood thinning medications
18 Years
85 Years
ALL
No
Sponsors
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Mayo Clinic
OTHER
Responsible Party
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Kenneth K. Wang
Kathy and Russ Van Cleve Professor of Gastroenterology Research
Principal Investigators
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Kenneth K Wang, MD
Role: PRINCIPAL_INVESTIGATOR
Mayo Clinic, Rochester, MN
Locations
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Mayo Clinic Rochester
Rochester, Minnesota, United States
Countries
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Related Links
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Mayo Clinic Clinical Trials
Other Identifiers
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07-006981
Identifier Type: -
Identifier Source: org_study_id