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NCT01028235 Clinical Trial

Routine Screening for Eosinophilic Esophagitis in Patients Presenting With Dysphagia

Dysphagia Clinical Trial

Official title:
Routine Screening for Eosinophilic Esophagitis in Patients Presenting With Dysphagia

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT01028235
Other study ID # FWH20060112H
Secondary ID
Status Recruiting
Phase N/A
First received December 8, 2009
Last updated December 8, 2009
Start date January 2006
Est. completion date January 2010

Study information
Verified date November 2009
Source San Antonio Uniformed Services Health Education Consortium
Contact Jonathan M Ricker, DO
Phone 210-292-6408
Email jonathan.ricker@lackland.af.mil
Is FDA regulated No
Health authority United States: Federal Government
Study type Observational

Clinical Trial Summary

The purpose of this study is to identify the prevalence of pathologic eosinophilic esophagitis (EoE) in the cohort of adult patients who present for specialty care in the gastroenterology clinics with complaint of difficulty swallowing (dysphagia). From this, the investigators will make recommendations regarding routine screening for the diagnosis in this cohort. The prevalence of EoE in patients presenting for specialty care in the gastroenterology clinics with the complaint of dysphagia is great enough that the diagnosis should be routinely screened against in this cohort.

Recruitment information / eligibility
Status Recruiting
Enrollment 150
Est. completion date January 2010
Est. primary completion date January 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- age > 18

- complaint of dysphagia

Exclusion Criteria:

- pregnancy

- 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)

Study Design

Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
United States Brooke Army Medical Center San Antonio Texas
United States Wilford Hall Medical Center San Antonio Texas

Sponsors (1)
Lead Sponsor Collaborator
San Antonio Uniformed Services Health Education Consortium

Country where clinical trial is conducted

United States, 

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