Posterior Approach to Total Shoulder Arthroplasty

Active, not recruiting

• Conditions: Osteo Arthritis Shoulders; Total Shoulder Arthroplasty

• Registration Number: NCT03623269
• Lead Sponsor: The Orthopaedic Research & Innovation Foundation

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.

Detailed Description

Not available

Study Timeline

• Study Start: 2017-10-01
• Study First Submitted: 2018-08-07
• Study First Submitted QC: 2018-08-07
• Study First Posted: 2018-08-09
• Status Verified: 2019-05
• Last Update Submitted: 2019-05-29
• Last Update Posted: 2019-05-30
• Primary Completion: 2023-08-31
• Study Completion: 2024-12-31

Recruitment & Eligibility

• Status: ACTIVE_NOT_RECRUITING
• Sex: All
• Target Recruitment: 31

Inclusion Criteria

1. English speaking
2. >18 years of age
3. Underwent posterior approach to total shoulder arthroplasty by Dr. Michael Greiwe at St. Elizabeth Healthcare

Exclusion Criteria

1. Non-English speaking
2. <18 years of age
3. Loose bone in the anterior recess of the shoulder
4. Severe arthritis with significant bony deformity

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
recovery	preoperative to 6 months postoperatively	range of motion
complications	6 months postoperative	percent of complications

Trial Locations

Locations (1)

The Orthopaedic Research & Innovation Foundation; 🇺🇸 Edgewood, Kentucky, United States