Optimization of Skin Preparation to Reduce Cutibacterium Acnes Colonization in Superficial and Deep Samples During Prosthetic Shoulder Surgery in Male Patients (OPRICA)

This is an interventional prevention trial for Cutibacterium Acnes Infection Read More

Inclusion Criteria:

• Male patients, Adult patients,
• Patient without a history of surgical intervention on the operated shoulder,
• Patient managed for glenohumeral, partial (cup or anatomical hemi- arthroplasty) or total (anatomical or inverted) glenohumeral arthroplasty placement for primary osteoarthritis, or secondary to necrosis, massive rotator cuff tear or old fracture.
• Patients affiliated to a social security system
• Patients who have given their informed and written consent

Exclusion Criteria:

• Patient with arthroplasty for resumption of previous shoulder surgery or failure of arthroplasty
• Patient with arthroplasty for acute trauma
• Patient on immunosuppressantsimmunosuppressive drugs
• Patient with inflammatory rheumatism
• Patient with progressive cancer pathology
• Allergies or intolerances concerning the modalities of selected skin preparations (Povidone Iodine, hypersensitivity to benzoyl peroxide)
• Dermatological pathologies in the area to be treated
• Acne treatment in the area to be treated within four weeks before inclusion
• Patient without possible help from a third party for the application of Cutacnyl® 5% in the intervention group if necessary
• Major under guardianship
• Patient under the protection of justice
• Patient not covered by social security