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N/A N=20 Treatment

Use of Real Time Instrumentation (RTI) in Total Shoulder Arthroplasty

Anatomic Total Shoulder Arthroplasty

Enrolled (actual)
20
Serious AEs
0.0%
Results posted
Jun 2021
Primary outcome: Primary: Difference in Glenoid Component Placement (Inclination and Version) — 2.0; 5.3 degrees

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Anatomic TSA using RTI (Device); Anatomic Total Shoulder Arthroplasty (Procedure)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
The Cleveland Clinic
Primary completion
Dec 2013

Outcome Measures

OutcomeResultp-value
PRIMARY
Difference in Glenoid Component Placement (Inclination and Version)
2.0; 5.3
PRIMARY
Difference in Glenoid Component Placement (AP and SP)
1.4; 1.1
SECONDARY
Difference in Glenoid Component Position Within and Between Surgeons
SECONDARY
Effect of Severity of Shoulder Pathology

Summary

Glenoid component loosening is the most common complication of total shoulder arthroplasty. Loosening is associated with malposition of the implant as well as the quality of the glenoid bone. Past studies from our research group have addressed these problems by investigating novel surgical technologies to increase the accuracy of glenoid implant placement. Over the course of multiple IRB approved clinical trials, use of our preoperative planning software in combination with patient specific instrumentation (PSI) or intelligent reusable instrumentation (IRI) has proven to more accurately place the glenoid guide pin than conventional standard of care techniques. Continuing the investigator's work, the investigators propose a clinical case series to evaluate a new surgical instrumentation technique that combines the features of PSI with the IRI technology that investigators have termed Real Time Instrumentation (RTI). Investigators will measure implant placement with RSA and 3D CT imaging. Investigators will measure pre-operative bone quality using quantitative CT to measure trabecular bone volume and correlate these findings with bone samples removed from the glenoid and measured by microCT and mechanical testing of the bone samples. These bone samples will be obtained as part of the routine preparation of the glenoid bone for implant placement. This bone tissue is normally removed and discarded as part of the standard of care for preparation of the bone for placement of the glenoid. Investigators have performed all of the work required to define both the safety of all components of the proposed study in the completed PSI study and the ongoing IRI study. Since application to the IRB for study of the IRI technology Custom Orthopaedic Solutions has received in April 2013 FDA approval for this technology.

Eligibility Criteria

Inclusion Criteria

  • To be eligible for inclusion, a primary anatomic total shoulder arthroplasty must be indicated for the patient.

Exclusion Criteria

  • Age less than 18.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01905241). 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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