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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03216135
Other study ID # 2017113
Secondary ID
Status Recruiting
Phase N/A
First received July 10, 2017
Last updated July 11, 2017
Start date July 20, 2017
Est. completion date December 2017

Study information

Verified date March 2017
Source Ochsner Health System
Contact Virendra Joshi, MD
Phone 504-842-7690
Email vjoshi@ochsner.org
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study will examine the hypothesis that altered esophageal microbiome leads to the development of esophageal adenocarcinoma (EAC). The aims of the project are, firstly the confirmation of relational data on the study cohort, using the methods developed and applied at the laboratory at University of Queensland Diamantina Institute (UQDI). Second, to generate a tissue microarray resource future tissue in-situ validation of microbes. And finally, to develop a biobank of clinical isolates of relevant esophageal microbes for future functional studies.


Description:

Gastroesophageal reflux disease, GERD, can lead to a change of the esophagus lining to a protective cell type, termed Barrett's esophagus (BE). A diagnosis of BE greatly increases the risk of developing esophageal adenocarcinoma (EAC). The incidence of EAC has been rapidly rising in the last 30 years, and the cancer has a high mortality rate. Understanding the involvement of the esophageal microbiota could lead to prevention strategies to this increasing health concern.

This study will examine the hypothesis that altered esophageal microbiome leads to the development of esophageal adenocarcinoma (EAC). The aims of the project are, firstly the confirmation of relational data on the study cohort, using the methods developed and applied at the laboratory at University of Queensland Diamantina Institute (UQDI). Second, to generate a tissue microarray resource future tissue in-situ validation of microbes. And finally, to develop a biobank of clinical isolates of relevant esophageal microbes for future functional studies.


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date December 2017
Est. primary completion date November 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Male or females >18 years of age with known or suspected GERD, Barrett's Esophagus and or esophageal adenocarcinoma or from patients who have a history of either condition.

Exclusion Criteria:

Study Design


Locations

Country Name City State
United States Ochsner Health System Kenner Louisiana

Sponsors (2)

Lead Sponsor Collaborator
Ochsner Health System The University of Queensland

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Microbial community profiling 16S Ribosomal RNA (rRNA)gene sequencing 9 months
Secondary Generate a tissue microarray After retrieval of blocks, an experienced pathologist will mark the relevant tissue areas to process into microarray 9 months
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