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Clinical Orthopaedic Data Bank (Acute and Chronic)

Sponsor
University of Florida (Other)
Overall Status
Recruiting
CT.gov ID
NCT00411060
Collaborator
(none)
10,000
Enrollment
1
Location
186
Duration (Months)
53.8
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

Data involving orthopaedic conditions and rehabilitation aspects of musculoskeletal and neuromuscular disorders will be collected and stored as part of the normal clinical care of patients seen in the University of Florida (UF) and Shands Orthopaedics and Sports Medicine Institute.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    All patients seen the Orthopaedic clinic will be informed of the data collection and asked to participate. If the patient is agreeable to participation, informed consent will then be obtained.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    10000 participants
    Observational Model:
    Other
    Time Perspective:
    Prospective
    Official Title:
    Orthopaedic Data Bank; Collection and Storage of Data Relating to Orthopaedic Disorders
    Study Start Date :
    Jan 1, 2007
    Anticipated Primary Completion Date :
    Jul 1, 2022
    Anticipated Study Completion Date :
    Jul 1, 2022

    Outcome Measures

    Primary Outcome Measures

    1. Retrospective data [2007 to present, until 2020]

      Medical Record information will be used as needed for a future IRB retrospective study

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • All patients seen in the UF&Shands Orthopaedics and Sports Medicine Institute will be asked to sign an informed consent.
    Exclusion Criteria:
    • No exclusions, all patients interested in participation will be asked to sign an informed consent.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 UF&Shands Orthopaedics and Sports Medicine Institute Gainesville Florida United States 32607

    Sponsors and Collaborators

    • University of Florida

    Investigators

    • Principal Investigator: Mark T. Scarborough, MD, UF Department of Orthopaedics and Rehabilitation

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    University of Florida
    ClinicalTrials.gov Identifier:
    NCT00411060
    Other Study ID Numbers:
    • IRB201501013
    • 117-2006
    • OCR18422
    First Posted:
    Dec 13, 2006
    Last Update Posted:
    Feb 12, 2021
    Last Verified:
    Feb 1, 2021
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by University of Florida
    Rotator Cuff Tear
    Additional relevant MeSH terms:
    Osteosarcoma
    Scoliosis
    Cerebral Palsy

    Study Results

    No Results Posted as of Feb 12, 2021