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N/A N=32

Prediction of Development of Scapular Notching Following Reverse Total Shoulder Arthroplasty

Osteoarthritis · Rotator Cuff Tear Arthropathy · Reverse Total Shoulder Arthroplasty · Scapular Notching

Enrolled (actual)
32
Serious AEs
20.0%
Results posted
Feb 2017
Primary outcome: Primary: Actual Versus Predicted Scapular Notching — 96.6 percentage of accurate predictions

Study Design & Population

Study type
Observational
Phase
N/A
Interventions
Age
Pediatric, Adult, Older Adult
Sex
All
Sponsor
Eric Ricchetti
Primary completion
Dec 2015

Outcome Measures

OutcomeResultp-value
PRIMARY
Actual Versus Predicted Scapular Notching
96.6
SECONDARY
Patient Reported Pain, Satisfaction and Function (Penn Shoulder Score)
78.4
SECONDARY
Shoulder Strength - Flexion
10.2
SECONDARY
Shoulder Strength - Abduction
11.3
SECONDARY
Shoulder Strength - Internal Rotation
9.7
SECONDARY
Shoulder Strength - External Rotation
7.5
SECONDARY
Active Shoulder Range of Motion - Flexion
134.5
SECONDARY
Active Shoulder Range of Motion - Abduction
120.5
SECONDARY
Active Shoulder Range of Motion - External Rotation
26.8
SECONDARY
Passive Shoulder Range of Motion - Flexion
141.7
SECONDARY
Passive Shoulder Range of Motion - Abduction
128.0
SECONDARY
Passive Shoulder Range of Motion - External Rotation
43

Summary

The hypothesis is that computer simulated bony impingement of the bone surrounding the spherical glenoid implant (the glenosphere) along the scapular neck on three-dimensional (3-D) computed tomography (CT) imaging analysis is predictive of the location of clinical scapular notching that develops following reverse total shoulder arthroplasty (TSA).

Eligibility Criteria

Inclusion Criteria

  • All patients having undergone reverse TSA at the Cleveland Clinic with a high quality preoperative CT of the operative shoulder and a minimum of two years out from surgery

Exclusion Criteria

  • All patients having undergone reverse TSA at the Cleveland Clinic with no preoperative CT or a low quality preoperative CT of the operative shoulder and/or less than two years from surgery
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02052466). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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