Outcomes Study of the Trabecular Metal (TM) Reverse Shoulder System

Rheumatoid Arthritis Clinical Trial

Official title:

Prospective Post Market Clinical Follow-up Study of the Zimmer Trabecular Metal Reverse Should System Used in Primary or Revision Reverse Total Shoulder Arthroplasty

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT01480440
• Other study ID #: CMU2010-28E
• Status: Active, not recruiting
• Start date: January 2011
• Est. completion date: December 2026

Study information

• Verified date: April 2024
• Source: Zimmer Biomet
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The objectives of this study are to obtain survival and outcome data on the Trabecular Metal Reverse Shoulder System when used in primary or revision reverse total shoulder arthroplasty.

Description:

The objectives of this study are to obtain survival and outcome data on the Trabecular Metal Reverse Shoulder System when used in primary or revision reverse total shoulder arthroplasty. This will be done by analysis of standard scoring systems, radiographs and adverse event records. Data will be collected and analyzed to monitor pain, function, and survivorship and to confirm the performance of the Trabecular Metal Reverse Shoulder System.

Performance will be evaluated by monitoring the frequency and incidence of adverse events as well as by assessment of the overall pain and functional performances, survivorship, health status and radiographic parameters of all enrolled study subjects who receive the Trabecular metal Reverse Shoulder System.

Pain and functional performance will be measured using the American Shoulder and Elbow Surgeons (ASES) Shoulder Assessment and the Single Assessment Numeric Evaluation (SANE), survivorship will be based on removal or intended removal of the device, health status will be determined by evaluation of the Short Form Survey12 (SF-12) as well as Adverse Events (AEs) and radiographic parameters analysis of x-rays.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 200
• Est. completion date: December 2026
• Est. primary completion date: December 2026
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patient is > 18 years of age;

• Patient is skeletally mature;

• Patient qualifies for primary or revision unilateral or bilateral reverse total shoulder arthroplasty based on physical exam and medical history including the following: osteoarthritis, rheumatoid arthritis, post-traumatic arthritis, ununited humeral head fracture, irreducible 3-and 4-part proximal humeral fractures, avascular necrosis, gross rotator cuff deficiency or failed total shoulder arthroplasty (both glenoid and humeral components require revision);

• Patient is willing and able to provide written informed consent;

• Patient is willing and able to cooperate in the required post-operative therapy;

• Patient is willing and able to complete scheduled follow-up evaluations/questionnaires as described in the Informed Consent;

• Patient has participated in the Informed Consent process and has signed the Institutional Review Board (IRB)/Ethical Review Board (ERB) approved informed consent.

Exclusion Criteria:

• The patient is a prisoner;

• The patient is mentally incompetent or unable to understand what participation in the study entails;

• The patient is a known alcohol or drug abuser;

• The patient is anticipated to be non-compliant;

• The patient has one of the following compromising the affected limb: a significant injury to the upper brachial plexus, paralysis of the axillary nerve or a neuromuscular disease compromising the affected limb which would render the procedure unjustifiable;

• The patient has a local/systemic infection;

• The patient is known to be pregnant;

• The patient has marked bone loss;

• The patient has a known sensitivity or allergic reaction to one or more of the implanted materials;

• The patient is unwilling or unable to give consent or to comply with the follow-up program.

Related Conditions & MeSH terms

• Arthritis
• Arthritis, Rheumatoid
• Avascular Necrosis
• Fractures, Bone
• Gross Rotator Cuff Deficiency
• Humeral Fractures
• Irreducible 3-and 4-part Proximal Humeral Fractures
• Necrosis
• Osteoarthritis
• Post-traumatic Arthritis
• Revision Total Shoulder Arthroplasty
• Rheumatoid Arthritis
• Shoulder Fractures
• Ununited Humeral Head Fracture

Intervention

Device:
• Trabecular Metal Reverse Shoulder System
Trabecular Metal Reverse Shoulder System used in primary or revision total shoulder arthroplasty

Locations

Country	Name	City	State
United Kingdom	Royal Blackburn Hospital	Blackburn	Lancashire
United States	The Rothman Institute	Egg Harbor Township	New Jersey
United States	Norton Orthopaedic & Sports Medicine	Louisville	Kentucky
United States	The Rothman Institute	Philadelphia	Pennsylvania
United States	University of California, San Francisco	San Francisco	California

Sponsors (1)

Lead Sponsor	Collaborator
Zimmer Biomet

Countries where clinical trial is conducted

United States,  United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Survivorship	Based on removal or intended removal of the device and determined using the Kaplan-Meier method.	10 Years
Secondary	Pain and Functional Performance	Measurements will be based on the American Shoulder and Elbow Surgeons (ASES) Shoulder Assessment and the Single Assessment Numeric Evaluation (SANE)	10 Years