Clinical Orthopaedic Data Bank (Acute and Chronic)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. Identifier: NCT00411060
Recruitment Status : Recruiting
First Posted : December 13, 2006
Last Update Posted : December 31, 2018
Information provided by (Responsible Party):
University of Florida

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
Osteoarthritis Osteosarcoma Scoliosis Cerebral Palsy

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 Type : Observational
Estimated 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 : January 2007
Estimated Primary Completion Date : January 2021
Estimated Study Completion Date : January 2021

Resource links provided by the National Library of Medicine

Primary Outcome Measures :
  1. Retrospective data [ Time Frame: 2007 to present, until 2020 ]
    Medical Record information will be used as needed for a future IRB retrospective study

Information from the National Library of Medicine

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Ages Eligible for Study:   Child, Adult, Older Adult
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Orthopaedic clinic

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.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT00411060

Contact: MaryBeth Horodyski, EdD 352-273-7379

United States, Florida
UF&Shands Orthopaedics and Sports Medicine Institute Recruiting
Gainesville, Florida, United States, 32607
Contact: MaryBeth Horodyski, EdD    352-273-7379   
Sponsors and Collaborators
University of Florida
Principal Investigator: Mark T. Scarborough, MD UF Department of Orthopaedics and Rehabilitation

Additional Information:
Responsible Party: University of Florida Identifier: NCT00411060     History of Changes
Other Study ID Numbers: IRB201501013
117-2006 ( Other Identifier: Legacy study )
OCR18422 ( Other Identifier: Universiy of Florida )
First Posted: December 13, 2006    Key Record Dates
Last Update Posted: December 31, 2018
Last Verified: December 2018

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:
Cerebral Palsy
Joint Diseases
Musculoskeletal Diseases
Rheumatic Diseases
Brain Damage, Chronic
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases
Neoplasms, Bone Tissue
Neoplasms, Connective Tissue
Neoplasms, Connective and Soft Tissue
Neoplasms by Histologic Type
Spinal Curvatures
Spinal Diseases
Bone Diseases