Patients who underwent arthroscopic rotator cuff repair at Siriraj hospital arthroscopic rotator cuff repair postoperative pain functional outcome radiofrequency device
Conditions
Interventions
Patients who underwent arthroscopic rotator cuff repair, in which radiofrequency device was used intraoperatively. All patients will be recorded for the time and energy usage of radiofrequency device
Supportive Care
Patients who underwent arthroscopic rotator cuff repair
Sponsors
Faculty of Medicine, Siriraj Hospital
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. Patients who underwent arthroscopic rotator cuff repair at Siriraj hospital 2. Age of more than 18 years old
Exclusion criteria
Exclusion criteria: 1. Patients who underwent other ligamentous procedures in the same surgery 2. Patients with previous fractures or dislocations of proximal humerus, clavicle or scapular region of the extremity involved in the study 3. Patients with neurological injury that interferes with postoperative pain of the extremity involved in this study 4. Patients unwilling to participate in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain assessment 2, 4, 6, 8, 12, 24, 48 hours and 1, 2 and 6 weeks postoperatively Numerical Rating Scale (NRS) | — |
Secondary
| Measure | Time frame |
|---|---|
| Opioid consumption rate Total opioid consumption in 48 hours postoperatively Morphine milligram equivalent (MME),Postoperative quality of life 6 weeks postoperatively Thai version of EQ-5D-5L | — |
Countries
Thailand
Contacts
Public ContactNut Kittipongphat
Faculty of Medicine, Siriraj Hospital, Mahidol University
Outcome results
None listed