Dislocation of the acromioclavicular joint
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Both genders; over 18 years of age; type III acromioclavicular dislocations with up to 21 days of evolution; absence of acromioclavicular dislocation in the shoulder in question; absence of previous surgery on the shoulder in question; absence of concomitant fracture of the acromion, coracoid or clavicle; signing the consent form.
Exclusion criteria
Exclusion criteria: Patients who did not meet the return schedule; patients in whom radiological examinations were not performed correctly; patients who did not comply with the proposed rehabilitation program.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary assessment tool will be the DASH, which consists of a 30-item scale ranging from 0 (no dysfunction) to 100. Patients undergoing surgical treatment are expected to present superior results. Patients will be evaluated at 3 weeks, 6 weeks, 3 months, 6 months and 1 year. The evaluations will be carried out by a member of the study and will be carried out with a shoulder covered with adhesive tape to allow the evaluator to be blinded in relation to the treatment performed. | — |
Secondary
| Measure | Time frame |
|---|---|
| Radiographic assessment. Patients undergoing surgical treatment are expected to present less arthritis at the acromioclavicular joint. Patients will be evaluated at 3 weeks, 6 weeks, 3 months, 6 months and 1 year. The evaluations will be carried out by a member of the study and will be carried out with a shoulder covered with adhesive tape to allow the evaluator to be blinded in relation to the treatment performed.;Range of motion assessment. Patients undergoing surgical treatment are expected to present superior results. Patients will be evaluated at 3 weeks, 6 weeks, 3 months, 6 months and 1 year. The evaluations will be carried out by a member of the study and will be carried out with a shoulder covered with adhesive tape to allow the evaluator to be blinded in relation to the treatment performed.;Cosmetic outcome. Patients undergoing surgical treatment are expected to present superior results. Patients will be evaluated at 3 weeks, 6 weeks, 3 months, 6 months and 1 year. The evaluations will be carried out by a member of the study and will be carried out with a shoulder covered with adhesive tape to allow the evaluator to be blinded in relation to the treatment performed.;Scapular dyskinesia, which will be graded according to Kibler's classification. Patients undergoing surgical treatment are expected to present superior results. Patients will be evaluated at 3 weeks, 6 weeks, 3 months, 6 months and 1 year. The evaluations will be carried out by a member of the study and will be carried out with a shoulder covered with adhesive tape to allow the evaluator to be blinded in relation to the treatment performed. | — |
Countries
Brazil
Contacts
Centro de Traumatologia do Esporte da Escola Paulista de Medicina