Acromioclavicular joint dislocation
Conditions
Interventions
This is a randomized clinical trial to be developed in a single center, with two randomized parallel groups. 18 participants will be included in each group, allocated in one of two groups (Surgical or
Sponsors
Fundação Faculdade de Medicina de São José do Rio Preto
Fundação Faculdade de Medicina de São José do Rio Preto
Eligibility
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Volunteers of both genders with grade III acromioclavicular dislocation; acute acromioclavicular dislocations; adults between 18 and 65 years old; no medical contraindications for the proposed treatments; acceptance and understanding of the informed consent form
Exclusion criteria
Exclusion criteria: Acromioclavicular dislocations grades I, II, IV, V and VI; dislocation with more than 14 days of evolution; associated neurovascular injury diagnosed on physical examination; head trauma; fracture in the ipsilateral upper limb; previous diseases in the affected limb that may influence the results; medical contraindication for surgery and/or anesthesia
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The function and symptoms presented by the participants with the method employed will be evaluated using the DASH questionnaire, Disabilities of the arm, shoulder and hand | — |
Secondary
| Measure | Time frame |
|---|---|
| Patient in need of surgical treatment for treatment of recurrent dislocation after surgical procedure, symptomatic deformity after conservative treatment or intractable pain;Adverse eventsThose patients with perception of cosmetic deformity will be considered with adverse events; with asymptomatic acromioclavicular instability; shoulder stiffness; other events reported by the patient;Dislocation recurrenceThose patients who, in the Zanca view, present an increase in the coracoclavicular space greater than 100% in relation to the contralateral side will be considered with recurrent dislocation after surgical treatment;UCLA-modified scores (Modified University of California at Los Angeles) will be used to assess function, satisfaction and quality of life ;SF-12 Questionnaire (Short form survey) will be used to assess quality of life after and during treatment ;Return time to activitiesThe return to pre-injury activities, such as work, sport, and usual daily activities, will be analyzed and presented according to the time elapsed between the trauma and the return, calculated in weeks ;Pain will be assessed using the Visual Analog Pain Scale (VAS) and the need for medication reported by the patient will also be analyzed | — |
Countries
Brazil
Contacts
Public ContactOreste Carrazzone
Fundação Faculdade de Medicina de São José do Rio Preto
Outcome results
None listed