Reverse Total Shoulder Arthroplasty With or Without Partial Coracoidectomy: Evaluation of Functional Internal Rotation

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

This trial does not accept healthy volunteers

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

Design model

Parallel

Treatments tested in this trial

  • Reverse total shoulder arthroplasty with coracoidectomy

    Procedure/Surgery

    Reverse total shoulder arthroplasty with coracoidectomy

  • Reverse total shoulder arthroplasty without coracoidectomy

    Procedure/Surgery

    Reverse total shoulder arthroplasty without coracoidectomy

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: Reverse total shoulder arthroplasty without coracoidectomySham comparator 1 intervention
Group B: Reverse total shoulder arthroplasty with coracoidectomyExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Assessment of functional internal rotation, as measured by the change in the ADLIR (Activities of Daily Living requiring Internal Rotation) score

A maximum score of 100 indicates that the patient experiences no discomfort in daily life due to limited internal rotation. A minimum score of 14 indicates severe functional impairment due to limited internal rotation.

Time frame
12 months after surgery

Secondary outcomes

Other outcomes

Sponsors and contacts

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