Radiologist-Integrated Finite Element Framework for Acromial Stress in Reverse Shoulder Arthroplasty

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age60-80
SponsorUniversity of Molise

About this trial

The current prospective single-center study is designed to examine an approach that utilizes both high-resolution CT and MRI scans, coupled with customized finite element modelling to analyze the stress placed on the acromion of patients who have undergone RSA surgery. The degree of rotator cuff deficiency will be assessed using Goutallier classification and quantified as Cuff Deficiency Index (CDI), which directly provides biomechanical information for calculating deltoid forces used in finite element analysis. Von Mises stresses will then be analyzed in anatomically defined acromial zones (Levy zones I-III).

Eligibility criteria

Qualifiers

Adult patients (60-80 years) with cuff tear arthropathy (Hamada grade 3 or above, Walch glenoid B/C) scheduled for primary unilateral reverse shoulder arthroplasty

Availability of preoperative high-resolution CT (voxel 1 mm or less) and 1.5T/3T MRI

Written informed consent for prospective use of anonymised data

Disqualifiers

Revision RSA or history of prior shoulder prosthetic complications

Uncorrectable imaging artefacts

Post-RSA follow-up shorter than 6 months

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

No trial groups listed

Sponsors and collaborators