Use of Simplified Pain Questionnaire Among People Receiving Anterior Cruciate Ligament (ACL) Knee Surgery?
Enrolling by invitation · Not applicable
Conditions studied: Anterior Cruciate Ligament (ACL) Reconstruction, Anterior Cruciate Ligament/Surgery
In brief
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.
Key facts
- Study ID
- NCT07065266
- Run by
- Stanford University
- People needed
- 130
- Starts
- 2020-07-24
- Expected to finish
- 2027-07-01
- Last updated by the study team
- 2026-06-15
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age 18+
- Undergoing ACL reconstruction surgery at Stanford Sports Medicine Redwood City, with autograft or allograft, with or without concomitant meniscal repair.
You may not qualify if…
- Pregnant women
- Surgical history of the operated knee
- Known allergy to opioid medications
- Received extra-routine pain care (as compared with the average ACL patients at the Sports Medicine division) given by the anesthesiologists, such as the postoperative epidural analgesia or the ultra-sound guided femoral nerve block.
Where it is running
- Stanford Orthopaedic and Sports Medicine — Redwood City, California, United States
Full record on ClinicalTrials.gov
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