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

This study has been completed.
Sponsor:
Information provided by:
University Hospital, Ghent
ClinicalTrials.gov Identifier:
NCT00284401
First received: January 30, 2006
Last updated: December 19, 2007
Last verified: December 2007
  Purpose

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 Intervention
Shoulder Prosthesis
Procedure: Evaluation of the placement of the Delta prosthesis

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: 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

Further study details as provided by University Hospital, Ghent:

Primary Outcome Measures:
  • Function and mobility of the shoulder

Estimated Enrollment: 50
Study Start Date: February 2004
Study Completion Date: July 2004
  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Shoulder prosthesis

Exclusion Criteria:

  • Inability to place the hand on the back in prone position
  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: NCT00284401

Locations
Belgium
University Hospital Ghent
Ghent, Belgium, 9000
Sponsors and Collaborators
University Hospital, Ghent
Investigators
Principal Investigator: Rene Verdonk, MD, PhD University Hospital, Ghent
  More Information

Additional Information:
No publications provided

ClinicalTrials.gov Identifier: NCT00284401     History of Changes
Other Study ID Numbers: 2004/102
Study First Received: January 30, 2006
Last Updated: December 19, 2007
Health Authority: Belgium: Institutional Review Board

Keywords provided by University Hospital, Ghent:
Reversed prosthesis

ClinicalTrials.gov processed this record on August 28, 2014