Status:
COMPLETED
Patient Specific Instruments Versus Standard Surgical Instruments
Lead Sponsor:
The Cleveland Clinic
Conditions:
Total Shoulder Arthroplasty
Eligibility:
All Genders
Phase:
NA
Brief Summary
Comparison of Glenoid Component Position Using Patient Specific Instruments Versus Standard Surgical Instruments: A Randomized Prospective Clinical Trial
Detailed Description
This is a non blinded prospective randomized clinical trial to define the efficacy of a new technology developed at the Cleveland Clinic to improve the positioning of the glenoid component in total sh...
Eligibility Criteria
Inclusion
- All patients otherwise indicated for primary reverse or anatomic total shoulder replacement that are able to get a pre-operative CT scan at the Cleveland Clinic will be considered eligible for enrollment. All patients will be consented in the office as part of the pre-operative consent for surgery and all will need to randomization at the time of surgery
Exclusion
- Patients will be excluded if they have significant metal in the joint that results in metal artifact on the CT scan, thereby compromising the ability to visualize the glenoid on the pre-operative simulator.
Key Trial Info
Start Date :
September 1 2010
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
May 1 2011
Estimated Enrollment :
44 Patients enrolled
Trial Details
Trial ID
NCT01430468
Start Date
September 1 2010
End Date
May 1 2011
Last Update
June 1 2020
Active Locations (1)
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1
Cleveland Clinic
Cleveland, Ohio, United States, 44195