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
75 participants
OBSERVATIONAL
2007-07-31
2009-03-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Eligibility Criteria
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Exclusion Criteria
Child Subjects: Any contraindication to endoscopy and biopsy, such as as liver dysfunction, history of bleeding, history of other serious organ disease (for example, kidney, heart, lung), bleeding time prolonged to over 10 minutes, or unexpected findings such as esophageal stricture that limits endoscopic examination will exclude subjects from the study, as will the use of antibiotics during the previous 2 weeks. In addition, if the endoscopist feels that prolonging the procedure by 2 or 3 minutes in order to take the research biopsies would not be advisable for any reason, the subject will be excluded from the study. Specific tests such as bleeding times will be performed at the discretion of the supervising clinician, who is undertaking the diagnostic endoscopy for the subject's clinical benefit.
6 Months
ALL
No
Sponsors
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National Institute of Allergy and Infectious Diseases (NIAID)
NIH
Medical Research Council Unit, The Gambia
OTHER
Responsible Party
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Principal Investigators
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Richard Adegbola, PhD, FRCPath
Role: PRINCIPAL_INVESTIGATOR
Medical Research Council Unit, The Gambia
Locations
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Medical Research Council's Laboratories
Banjul, , The Gambia
Countries
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Other Identifiers
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06-0053
Identifier Type: -
Identifier Source: org_study_id
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