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Clinical Orthopaedic Data Bank (Acute and Chronic)

This study is currently recruiting participants. (see Contacts and Locations)
Verified November 2014 by University of Florida
Sponsor:
Information provided by (Responsible Party):
University of Florida
ClinicalTrials.gov Identifier:
NCT00411060
First received: December 12, 2006
Last updated: November 13, 2014
Last verified: November 2014
  Purpose

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
Osteoarthritis
Osteosarcoma
Scoliosis
Cerebral Palsy

Study Type: Observational
Study Design: Time Perspective: Prospective
Official Title: Orthopaedic Data Bank; Collection and Storage of Data Relating to Orthopaedic Disorders

Resource links provided by NLM:


Further study details as provided by University of Florida:

Primary Outcome Measures:
  • Retrospective data [ Time Frame: 2007 to present, until 2020 ] [ Designated as safety issue: No ]
    Medical Record information will be used as needed for a future IRB retrospective study


Estimated Enrollment: 10000
Study Start Date: January 2007
Estimated Study Completion Date: January 2020
Estimated Primary Completion Date: January 2020 (Final data collection date for primary outcome measure)
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.

  Eligibility

Genders Eligible for Study:   Both
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.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: 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
  More Information

Additional Information:
No publications provided

Responsible Party: University of Florida
ClinicalTrials.gov Identifier: NCT00411060     History of Changes
Other Study ID Numbers: 117-2006
Study First Received: December 12, 2006
Last Updated: November 13, 2014
Health Authority: United States: Institutional Review Board

Keywords provided by University of Florida:
Rotator Cuff Tear

Additional relevant MeSH terms:
Cerebral Palsy
Osteoarthritis
Osteosarcoma
Arthritis
Brain Damage, Chronic
Brain Diseases
Central Nervous System Diseases
Joint Diseases
Musculoskeletal Diseases
Neoplasms
Neoplasms by Histologic Type
Neoplasms, Bone Tissue
Neoplasms, Connective Tissue
Neoplasms, Connective and Soft Tissue
Nervous System Diseases
Rheumatic Diseases
Sarcoma

ClinicalTrials.gov processed this record on November 20, 2014