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Clinical Trials/NCT03623269
NCT03623269
Active, not recruiting
Not Applicable

Posterior Approach to Total Shoulder Arthroplasty: A Data Analysis on Patients Undergoing the Posterior Approach to Total Shoulder Arthroplasty

The Orthopaedic Research & Innovation Foundation1 site in 1 country31 target enrollmentOctober 1, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Total Shoulder Arthroplasty
Sponsor
The Orthopaedic Research & Innovation Foundation
Enrollment
31
Locations
1
Primary Endpoint
complications
Status
Active, not recruiting
Last Updated
6 years ago

Overview

Brief Summary

The purpose of this study is to evaluate preoperative objective measurements and operative objective measurements to determine if there is any effect to postoperative outcomes. Patients who were 18 years old or greater at the time of surgery were followed clinically and radiographically to determine best practice and optimal treatment and technique, risk and rate of complication, and postoperative outcomes.

Registry
clinicaltrials.gov
Start Date
October 1, 2017
End Date
December 31, 2024
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
The Orthopaedic Research & Innovation Foundation
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • English speaking
  • \>18 years of age
  • Underwent posterior approach to total shoulder arthroplasty by Dr. Michael Greiwe at St. Elizabeth Healthcare

Exclusion Criteria

  • Non-English speaking
  • \<18 years of age
  • Loose bone in the anterior recess of the shoulder
  • Severe arthritis with significant bony deformity

Outcomes

Primary Outcomes

complications

Time Frame: 6 months postoperative

percent of complications

recovery

Time Frame: preoperative to 6 months postoperatively

range of motion

Study Sites (1)

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