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Clinical Orthopaedic Data Bank (Acute and Chronic)

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ClinicalTrials.gov Identifier: NCT00411060
Recruitment Status : Recruiting
First Posted : December 13, 2006
Last Update Posted : December 8, 2017
Sponsor:
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 2020
Estimated Study Completion Date : January 2020

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
Criteria

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 ClinicalTrials.gov identifier (NCT number): NCT00411060


Contacts
Contact: MaryBeth Horodyski, EdD 352-273-7379 horodmb@ortho.ufl.edu

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

Additional Information:
Responsible Party: University of Florida
ClinicalTrials.gov Identifier: NCT00411060     History of Changes
Other Study ID Numbers: IRB201501013
117-2006 ( Other Identifier: Legacy study )
First Posted: December 13, 2006    Key Record Dates
Last Update Posted: December 8, 2017
Last Verified: December 2017

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
Osteoarthritis
Cerebral Palsy
Scoliosis
Arthritis
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
Neoplasms
Sarcoma
Spinal Curvatures
Spinal Diseases
Bone Diseases