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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT03803527
Other study ID # 19-0074
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date December 1, 2019
Est. completion date August 1, 2021

Study information

Verified date October 2019
Source University of Colorado, Denver
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A prospective longitudinal, observational study of adolescent and adults that will identify novel metabolites associated with dysphagia in Eosinophilic Esophagitis (EoE).


Description:

In this study, the investigators seek to understand whether a metabolomic profile obtained from esophageal samples correlate with the symptom of dysphagia in adolescent and adults. The investigators hypothesize that intraluminal secreted metabolite(s) will change during episodes of dysphagia. The aim of the study will be to use a novel method of producing esophageal luminal samples, the esophageal string test, to capture esophageal metabolites when a patient is and is not experiencing dysphagia.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date August 1, 2021
Est. primary completion date February 1, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 11 Years to 55 Years
Eligibility Inclusion Criteria:

- Subjects with Eosinophilic Esophagitis (EoE) and seen either at Children's Hospital Colorado or University of Colorado Hospital for scheduled outpatient clinical assessment or upper GI endoscopy

Exclusion Criteria:

- Acute food impaction at time of study

- Recent (within 2 months) use of systemic steroids

- Other known esophageal disease or esophageal injury (e.g. tracheoesophageal fistula, congenital stricture, caustic injury)

- known other inflammatory bowel disease

- inability to swallow the EST

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Esophageal String Test
An EST will be performed for a 1hour sampling period on the same day as the scheduled clinic visit. Subjects will be asked to swallow a capsule and the attached EST string will be taped to the cheek with tegaderm tape. At the completion of the 1-hour sampling period, the EST will be removed and it will immediately be processed and cryopreserved for metabolomics profiling.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of Colorado, Denver

Outcome

Type Measure Description Time frame Safety issue
Primary Brief Esophageal Dysphagia Questionnaire Positive Dysphagia symptoms Measured by Brief Esophageal Dysphagia Questionnaire. The questionnaire asks questions about dysphagia symptoms and the scale is from 0 (rarely/never) to 5 (several times per day). Time of Endoscopic Procedure
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