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GI Biorepository of Tissue and Bodily Fluids

Sponsor
University of California, Davis (Other)
Overall Status
Completed
CT.gov ID
NCT02486146
Collaborator
(none)
789
Enrollment
1
Location
30
Duration (Months)
26.3
Patients Per Site Per Month

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase

    Detailed 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.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    789 participants
    Observational Model:
    Other
    Time Perspective:
    Prospective
    Official Title:
    GI Biorepository of Tissue and Bodily Fluids
    Study Start Date :
    Oct 1, 2014
    Actual Primary Completion Date :
    Apr 1, 2017
    Actual Study Completion Date :
    Apr 1, 2017

    Outcome Measures

    Primary Outcome Measures

    1. To build a model biorepository to streamline the biobanking process and provide centralized specimens and associated health information for translational research. [4 years]

      To have biospecimens available for the UC Davis IRB approved studies.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 85 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    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.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 UC Davis Health System Sacramento California United States 95817

    Sponsors and Collaborators

    • University of California, Davis

    Investigators

    • Principal Investigator: Yu-Jui Yvonne Wan, PhD, University of California, Davis

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University of California, Davis
    ClinicalTrials.gov Identifier:
    NCT02486146
    Other Study ID Numbers:
    • 575191
    First Posted:
    Jul 1, 2015
    Last Update Posted:
    Jun 21, 2017
    Last Verified:
    Jun 1, 2017
    Additional relevant MeSH terms:
    Gastrointestinal Diseases
    Digestive System Diseases

    Study Results

    No Results Posted as of Jun 21, 2017