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Prosthetic Component Relationship of the Reversed Delta III Total Shoulder Prosthesis in the Transverse Plane of the Body

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.
 
ClinicalTrials.gov Identifier: NCT00284401
Recruitment Status : Completed
First Posted : January 31, 2006
Last Update Posted : December 28, 2007
Sponsor:
Information provided by:
University Hospital, Ghent

Brief Summary:
Comparison of the function and mobility of the shoulder with the placement of the Delta prosthesis (anteversion and retroversion of the glenoidal and humeral components)

Condition or disease Intervention/treatment Phase
Shoulder Prosthesis Procedure: Evaluation of the placement of the Delta prosthesis Not Applicable

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Study Type : Interventional  (Clinical Trial)
Enrollment : 50 participants
Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Prosthetic Component Relationship of the Reversed Delta III Total Shoulder Prosthesis in the Transverse Plane of the Body
Study Start Date : February 2004
Actual Study Completion Date : July 2004

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Artificial Limbs




Primary Outcome Measures :
  1. Function and mobility of the shoulder


Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Shoulder prosthesis

Exclusion Criteria:

  • Inability to place the hand on the back in prone position

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): NCT00284401


Locations
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Belgium
University Hospital Ghent
Ghent, Belgium, 9000
Sponsors and Collaborators
University Hospital, Ghent
Investigators
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Principal Investigator: Rene Verdonk, MD, PhD University Hospital, Ghent
Additional Information:
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ClinicalTrials.gov Identifier: NCT00284401    
Other Study ID Numbers: 2004/102
First Posted: January 31, 2006    Key Record Dates
Last Update Posted: December 28, 2007
Last Verified: December 2007
Keywords provided by University Hospital, Ghent:
Reversed prosthesis