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The purpose of this study is to develop and test an opioid-free pain control protocol for patients undergoing arthroscopic rotator cuff repair.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Arthroscopic Rotator Cuff Repair |
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| Measure | Description | Time Frame |
|---|---|---|
| Time to fulfill oxycodone prescription | data collected to the time from surgery until the patient chooses to fulfill a prescription for opioid medication following surgery | within first 3 days of surgery |
| Measure | Description | Time Frame |
|---|---|---|
| VAS pain (Visual Analog Scale) | patient-reported pain as measured on a scale from 0-10. Zero means no pain and 10 being worst pain imaginable | Post-operative day 3 |
| Patient satisfaction | Patient will be asked on a 5 point likert scale to rate their satisfaction with their post-operative pain regime |
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Inclusion Criteria:
Exclusion Criteria:
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patients undergoing ARCR will be asked to participate in this survey study
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Rothman Institute | Philadelphia | Pennsylvania | 19148 | United States |
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| ID | Term |
|---|---|
| D000070636 | Rotator Cuff Injuries |
| ID | Term |
|---|---|
| D012421 | Rupture |
| D014947 | Wounds and Injuries |
| D000070599 | Shoulder Injuries |
| D013708 | Tendon Injuries |
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| Post-operative day 3 |