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Uncemented Total Elbow Arthroplasty Data Collection

This study has been terminated.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00974298
First Posted: September 10, 2009
Last Update Posted: August 6, 2014
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. Read our disclaimer for details.
Information provided by (Responsible Party):
Donald Lee, Vanderbilt University
  Purpose
The purpose of this study is to document the performance and clinical outcomes of uncemented total elbow replacements involving the press-fit technique performed at the Vanderbilt Hand Center. The press-fit use technique is often used because of complications with cement loosening.

Condition Intervention
Total Elbow Arthroplasty Procedure: Total elbow replacement arthroplasty

Study Type: Observational
Study Design: Time Perspective: Prospective
Official Title: Uncemented Total Elbow Arthroplasty Data Collection

Further study details as provided by Donald Lee, Vanderbilt University:

Primary Outcome Measures:
  • Patient examination measurements and radiographic measurements will be used to determine the effects of an uncemented total elbow arthroplasty [ Time Frame: Pre-operative to five year post-operative appointment ]

Enrollment: 2
Study Start Date: March 2009
Study Completion Date: December 2013
Primary Completion Date: December 2013 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
Elbow replacement
There are no other arms other then an uncemented total elbow replacement.
Procedure: Total elbow replacement arthroplasty
Total elbow arthroplasty using pressfit technique in which no cement is used.

Detailed Description:

The three parts of this study will be:

Retrospective Chart Review-

A chart review will be completed on all patients that have had an uncemented total elbow arthroplasty using the press-fit technique at Vanderbilt Hand & Upper Extremity Center. The chart review will include:

  • A historical data form
  • An operative data form
  • A radiographic assessment form

Questionnaire Mailing- We will mail prospective study patients a DASH (Disabilities of the Arm, Shoulder and Hand) questionnaire to complete with a mailing letter explaining the request for this information. The DASH will be modified to ask patients regarding their pre-operative time as well.

Clinical Data Collection-

We will enroll patients who have already had/or will be having a uncemented total elbow arthroplasty using the press-fit technique. If the patient already has a file completed through the chart review we will not complete the historical data form, operative form, or previous radiograph assessments. If the patient does not have a file completed through the chart review the data collection will include:

  • An Informed Consent Document
  • A historical data form
  • An operative data form
  • A radiographic assessment form
  • Patient-completed DASH questionnaire
  • Elbow Assessment Form
  Eligibility

Information from the National Library of Medicine

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, Learn About Clinical Studies.


Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients who require total elbow arthroplasty.
Criteria

Inclusion Criteria:

  • Any patient who has had a total elbow arthroplasty using a press-fit technique at the Vanderbilt Hand & Upper Extremity Center

Exclusion Criteria:

  • Patients less than 18 years old
  • For chart review and post-operative enrollment the patients must have adequate radiographs.
  Contacts and Locations
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): NCT00974298


Locations
United States, Tennessee
Vanderbilt University Hand & Upper Extremity Center
Nashville, Tennessee, United States, 37232-8828
Sponsors and Collaborators
Vanderbilt University
Investigators
Principal Investigator: Donald Lee, M.D. Vanderbilt University
  More Information

Responsible Party: Donald Lee, Professor of Orthopaedic Surgery, Vanderbilt University
ClinicalTrials.gov Identifier: NCT00974298     History of Changes
Other Study ID Numbers: 090342
First Submitted: September 2, 2009
First Posted: September 10, 2009
Last Update Posted: August 6, 2014
Last Verified: August 2014