Routine Screening for Eosinophilic Esophagitis in Patients Presenting With Dysphagia
NCT ID: NCT01028235
Last Updated: 2009-12-09
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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UNKNOWN
150 participants
OBSERVATIONAL
2006-01-31
2010-01-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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PROSPECTIVE
Study Groups
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Obstructive Dysphagia
Patients who complained of dysphagia, which had an obstructive etiology for their symptoms at the time of endoscopy (ring, mass, stricture, etc)
No interventions assigned to this group
Non-obstructive Dysphagia
Patients whose endoscopy was normal and without any obvious etiology for their symptoms noted.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* complaint of dysphagia
Exclusion Criteria
* age \<18
* on inhaled steroids within the last 30 days
* on systemic steroids in the last 30 days
* known diagnosis of Eosinophilic Esophagitis
* obvious obstructive etiology found at endoscopy
* increased risk of bleeding (on blood thinners or anti-platelet agents other than aspirin)
18 Years
ALL
Yes
Sponsors
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San Antonio Uniformed Services Health Education Consortium
FED
Responsible Party
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SAUSHEC
Principal Investigators
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Jonathan M Ricker, DO
Role: PRINCIPAL_INVESTIGATOR
San Antonio Uniformed Services Health Education Consortium
Locations
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Wilford Hall Medical Center
San Antonio, Texas, United States
Brooke Army Medical Center
San Antonio, Texas, United States
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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FWH20060112H
Identifier Type: -
Identifier Source: org_study_id
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