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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04069429
Other study ID # IRB_00058734
Secondary ID
Status Completed
Phase Early Phase 1
First received
Last updated
Start date July 2016
Est. completion date October 2020

Study information

Verified date April 2021
Source University of Utah
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a research study of a new agent used for evaluation of inflammation in the GI tract. This agent is investigational and thus is being studied to determine appropriate dosing and administration in both normal controls (i.e. people without gastrointestinal complaints) and patients with eosinophilic disease (i.e. those with an immune reaction and inflammation in their bodies with a certain cell called an eosinophil). The study will test whether the radiolabeled agent will bind to the inflammation of eosinophilic esophagitis patients because an animal model of eosinophilic esophagitis which shows the striking deposition of eosinophil granule proteins is not available.


Recruitment information / eligibility

Status Completed
Enrollment 8
Est. completion date October 2020
Est. primary completion date September 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - 10 patients with diagnosed EoE (greater than 20 eosinophils per HPF) on esophageal biopsy will be included as the diseased population - 7 controls (subjects without GI symptoms and known GI disease) Exclusion Criteria: - bleeding diathesis or contraindication to esophageal biopsies - severe sleep apnea - incarceration - pregnancy - inability to lie flat for 2 hours - history of bleeding disorder - Use of steroids - Breast feeding - Allergy to heparin or history of severe reaction to heparin - allergy to mucomyst or severe asthma

Study Design


Related Conditions & MeSH terms


Intervention

Radiation:
Computerized Tomography scan
imaging scan from a person's eyes to their thighs
Single Photon Emission Computed Tomography scans
imaging scan taken during, and after, the administration of the radioactive agent
Drug:
Technetium Tc 99M
subjects are administered radioactive heparin as part of study participation.
Radiation:
Planar Images
2 dimensional imaging - whole body planar scans
Procedure:
Esophagogastroduodenoscopy
esophagogastroduodenoscopy with tissue biopsies

Locations

Country Name City State
United States University of Utah Salt Lake City Utah

Sponsors (1)

Lead Sponsor Collaborator
University of Utah

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Biodistribution of Tc99m-heparin Biodistribution of Tc99m-heparin to the esophagus and other organs, especially of the gastrointestinal tract as judged by planar scans and by single photon emission computed tomography scans. over approximately 24-26 hours
Primary Calculation of organ doses Calculation of organ doses from the oral administration of Tc99m-heparin. The organ doses will be measured in miliSieverts using a computer program called OLINDA (Version 2). over approximately 24-26 hours
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