DenCT Shoulder Bone Quality Evaluation
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorZimmer Biomet
About this trial
The objective of the study is to evaluate the preoperative bone quality assessment based on CT to later establish a scale for the decision of stemless shoulder arthroplasty.
Eligibility criteria
Qualifiers
Patient must be older than 18 years and skeletally mature.
Patient must undergo the SHA, TSA, or RSA according to the Instructions for Use (IFU).
Patient must be anatomically and structurally suited to receive shoulder arthroplasty implants.
Non-inflammatory degenerative joint disease including osteoarthritis.
Disqualifiers
Fractures of the proximal humerus, where other methods of treatment are deemed inadequate.
Revision TSA/RSA after the prior TSA/RSA.
Patient has experienced the traumatic fractures to the implant site.
Patient is unwilling or unable to give consent
Trial design
Treatments tested in this trial
- Preoperative CT Scan
Treatment groups
200 Participants
are divided into 1 treatment groupSponsors and collaborators
Zimmer Biomet
Lead sponsor
Zimmer, GmbH
Collaborator
Source ClinicalTrials.gov