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

Shoulder Prosthesis Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00284401
• Other study ID #: 2004/102
• Status: Completed
• Phase: N/A
• First received: January 30, 2006
• Last updated: December 19, 2007
• Start date: February 2004
• Est. completion date: July 2004

Study information

• Verified date: December 2007
• Source: University Hospital, Ghent
• Contact: n/a
• Is FDA regulated: No
• Health authority: Belgium: Institutional Review Board
• Study type: Interventional

Clinical Trial 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)

Recruitment information / eligibility

• Status: Completed
• Enrollment: 50
• Est. completion date: July 2004
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Shoulder prosthesis

Exclusion Criteria:

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

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Shoulder Prosthesis

Intervention

Procedure:
• Evaluation of the placement of the Delta prosthesis

Locations

Country	Name	City	State
Belgium	University Hospital Ghent	Ghent

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital, Ghent

Country where clinical trial is conducted

Belgium, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Function and mobility of the shoulder

External Links

•   Website University Hospital Ghent