Randomized clinical trial of Proximal humeral fractures in three or four parts in elderly: Blocked plate with or without Synthetic graft augmentatio
- Conditions
- pper end humerus fractureC26.404.625
- Registration Number
- RBR-5v39tf8
- Lead Sponsor
- Instituto de Assistência Médica ao Servidor Público Estadual - IAMSPE
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- Not specified
Male and female patients; with proximal humeral fractures in 3 or 4 parts; involvement of the surgical neck; tuberosities deviation greater than 0.5 cm; contact between the diaphysis and the humeral head fragment smaller then fifty percent; patient aged over or equal to sixty years old; maximum time of fracture of 14 days
Patient's non-agreement to sign the free and informed consent form; 1- or 2-part fractures; dislocation fractures; pathological fractures; open fractures; associated fractures; head split joint fractures; patient's inability to understand the questionnaires; active or previous shoulder infections; nerve injury in the limb; infeasibility of perform osteosynthesis; irreparable rotator cuff injuries; previous shoulder surgeries; smoking; patients who do not agree with the surgical indication; any affection of the proximal end of the contralateral humerus that changes it's anatomy
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method