ConditionReverse Total Shoulder Arthroplasty
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorClinique Générale dAnnecy
About this trial
This project aims to conduct a randomized controlled trial comparing the functional outcomes and complications of standard reverse total shoulder arthroplasty and reverse total shoulder arthroplasty combined with partial coracoidectomy. The study will assess functional internal rotation at 12 months post-surgery, as measured by the ADLIR (Activities of Daily Living requiring Internal Rotation) score.
Eligibility criteria
Qualifiers
None
Disqualifiers
Patients with a history of coracoid fractures or who have previously undergone surgery involving the coracoid process.
Patients undergoing latissimus dorsi transfers
Presence of an active infection, inflammatory arthritis, or a tumor affecting the shoulder region.
Patients with pre-existing neuromuscular disorders affecting shoulder function
Trial design
Treatments tested in this trial
- Reverse total shoulder arthroplasty with coracoidectomy
- Reverse total shoulder arthroplasty without coracoidectomy
Treatment groups
60 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov