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The goal of this randomized clinical trial is to compare opioid consumption among patients who receive a binary pain scale compared to those who receive a standard 10-point pain scale after undergoing anterior cruciate ligament (ACL) reconstruction surgery.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 10-point pain scale | Active Comparator | participants undergoing ACL reconstructive surgery are asked to use a 10-point NPRS pain scale to describe their pain post-operatively |
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| Binary pain questionnaire | Experimental | Participants undergoing ACL reconstructive surgery are asked to describe their pain as tolerable or intolerable post-operatively |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Binary pain questionnaire | Other | Post-operative questionnaire that asks if pain is 'tolerable' or 'intolerable' |
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| Measure | Description | Time Frame |
|---|---|---|
| Amount of opioid medication used post-operatively for 14 days | 14 days post-surgery |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Todd Alamin, MD | Stanford University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Stanford Orthopaedic and Sports Medicine | Redwood City | California | 94063 | United States |
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| Numerical Pain Rating Scale (NPRS) | Other | Standard 10-point pain scale used post-operatively to assess pain |
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