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Ascension® Humeral Resurfacing Arthroplasty (HRA) Follow-Up Study — HRA  

Arthritis Clinical Trial

Official title:
Ascension® Humeral Resurfacing Arthroplasty HRA Follow-Up Study

Clinical Trial Summary

This is a prospective study on the Ascension HRA device to collect data to assess the safety and effectiveness of the HRA.

Clinical Trial Description

This study protocol will provide guidance to investigators wanting to perform a non-randomized, consecutive enrollment, 10-year follow-up study of patients who are treated with the Ascension® HRA. Its purpose is to measure and document the outcomes associated with implanting the Ascension HRA prosthesis. Patients will be periodically assessed to collect data related to safety and effectiveness endpoints at the following intervals: preoperative, surgery/immediate post-op, 3 months, 6 months, 1 year, 2 year, 5 year, and 10 years. ;

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02369497
Study type Observational
Source Integra LifeSciences Corporation
Contact
Status Terminated
Phase N/A
Start date December 2007
Completion date July 2014
View Details
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