Stanford Orthopaedic and Sports Medicine
Redwood City, California, 94063, United States
NCT Number: NCT07065266
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.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
Redwood City, California, 94063, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Post-operative questionnaire that asks if pain is 'tolerable' or 'intolerable'
Standard 10-point pain scale used post-operatively to assess pain
Time frame: 14 days post-surgery
Stanford University
Other
The Utility of a Dichotomous Pain Scale in Reducing Postoperative Opioids Consumption in Outpatient ACL Surgery: A Prospective Randomized Controlled Study
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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