Clinical Orthopaedic Data Bank (Acute and Chronic)

August 31, 2026 updated by: University of Florida

Orthopaedic Data Bank; Collection and Storage of Data Relating to Orthopaedic Disorders

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.

Study Overview

Status

Recruiting

Conditions

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

Enrollment (Estimated)

10000

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Name: MaryBeth Horodyski, EdD
Phone Number: 352-273-7379
Email: horodmb@ortho.ufl.edu

Study Locations

United States
- Florida
  - Gainesville, Florida, United States, 32607
    - Recruiting
    - UF&Shands Orthopaedics and Sports Medicine Institute
    - Contact:
      
      MaryBeth Horodyski, EdD
      
      Phone Number: 352-273-7379
      
      Email: horodmb@ortho.ufl.edu

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

Child
Adult
Older Adult

Accepts Healthy Volunteers

Sampling Method

Non-Probability Sample

Study Population

Orthopaedic clinic

Description

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 Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Retrospective data Time Frame: 2007 to present, until 2020	Medical Record information will be used as needed for a future IRB retrospective study	2007 to present, until 2020

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

University of Florida

Investigators

Principal Investigator: Parker Gibbs, MD, UF Department of Orthopaedics and Rehabilitation

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Helpful Links

University of Florida Department of Orthopaedics Research

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

January 1, 2007

Primary Completion (Estimated)

August 14, 2027

Study Completion (Estimated)

August 14, 2027

Study Registration Dates

First Submitted

December 12, 2006

First Submitted That Met QC Criteria