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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00411060
Other study ID # IRB201501013
Secondary ID 117-2006OCR18422
Status Recruiting
Phase
First received
Last updated
Start date January 2007
Est. completion date July 14, 2025

Study information

Verified date July 2023
Source University of Florida
Contact MaryBeth Horodyski, EdD
Phone 352-273-7379
Email horodmb@ortho.ufl.edu
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Recruiting
Enrollment 10000
Est. completion date July 14, 2025
Est. primary completion date July 14, 2025
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States UF&Shands Orthopaedics and Sports Medicine Institute Gainesville Florida

Sponsors (1)

Lead Sponsor Collaborator
University of Florida

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Retrospective data Medical Record information will be used as needed for a future IRB retrospective study 2007 to present, until 2020
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