Arthroscopic rotator cuff repair. Injury of muscle(s) and tendon(s) of the rotator cuff of shoulder
Conditions
Interventions
Intervention 1: First intervention group: 20 cc of bupivacaine, 0.25% of 40 micrograms of epinephrine will be injected into the sub acromial space space after surgery. Intervention 2: Second intervent
Sponsors
Yazd University of Medical Sciences
Eligibility
Sex/Gender
All
Age
30 Years to 80 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: Diagnosis of rotator cuff rupture clinically and MRI result. Conscious consent of the participants, Patients who are able to read and write.
Exclusion criteria
Exclusion criteria: Exclusion criteria: Patients with corrective or secondary surgery, patients with a history of trauma in the last 3 months, patients who have other surgeries in addition to rotator cuff repair, Patients who have mental health problems.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Post-operative pain score. Timepoint: Pain before and after surgery and up to 3 days after surgery. Method of measurement: Questionnaire, Visual Analogue Scale. | — |
Secondary
| Measure | Time frame |
|---|---|
| Hours of sleep. Timepoint: Pre-operative and post-operative. Method of measurement: questionnaire, The sleep time is entered into the clock in the questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAmin Adeli Mirzaei
Yazd University of Medical Sciences
Outcome results
None listed