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Prospective, randomized clinical trial investigating the use of patient education on post-operative narcotic consumption
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Normal pre-operative education | No Intervention | • Control group received normal pre-operative education regarding surgery | |
| Opioid usage education | Active Comparator | • The study group received formal education detailing recommended post-operative opioid usage, side effects, dependence, and addiction |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Formal education regarding opioid usage | Other | Participannts watched a 2 minute video and were given educational materials |
|
| Measure | Description | Time Frame |
|---|---|---|
| Opioid Usage | count of total narcotic pills not taken by patients | 3 months |
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Inclusion Criteria:
Exclusion Criteria:
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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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