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NCT02486146 Clinical Trial

GI Biorepository of Tissue and Bodily Fluids

Gastrointestinal Diseases Clinical Trial

Official title:
GI Biorepository of Tissue and Bodily Fluids

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02486146
Other study ID # 575191
Secondary ID
Status Completed
Phase N/A
First received June 19, 2015
Last updated June 19, 2017
Start date October 2014
Est. completion date April 2017

Study information
Verified date June 2017
Source University of California, Davis
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to establish the working protocols for a general biorepository with the specific aim of procuring tissues and bodily fluids from the human gastrointestinal tract from a diverse range of clinical patients at the UC Davis Medical Center. The establishment of a GI-specific biorepository will support future translational endeavors within the UC Davis campus by providing laboratories with readily available GI tissue and bodily fluid samples to test newly developed hypotheses with relative ease.

Description:

UC Davis is currently lacking a general use biorepository for GI tissues and bodily fluids. As with any translational research study, the procurement of human tissue samples can be a difficult and time- consuming process. The establishment of this biorepository will help streamline GI biospecimen collection and centralize these samples in a conveniently located space to facilitate the implementation of future unspecified translational studies.

Recruitment information / eligibility
Status Completed
Enrollment 789
Est. completion date April 2017
Est. primary completion date April 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria:

- all consenting adults aged 18 years or older with an appointment with a healthcare professional in the Division of Gastroenterology or the Department of Surgery

Exclusion Criteria:

- minors, pregnant women, prisoners, and all other vulnerable populations who are unable to consent.

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United States UC Davis Health System Sacramento California

Sponsors (1)
Lead Sponsor Collaborator
University of California, Davis

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary To build a model biorepository to streamline the biobanking process and provide centralized specimens and associated health information for translational research. To have biospecimens available for the UC Davis IRB approved studies. 4 years
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