NCT07065266
Use of Simplified Pain Questionnaire Among People Receiving Anterior Cruciate Ligament (ACL) Knee Surgery?
Enrolling by Invitation
NAAges 18+InterventionalStanford UniversityInvestigator-initiated
~130 participants
Updated 2026-06-15 on ClinicalTrials.gov
What's tested:Binary pain questionnaireNumerical Pain Rating Scale (NPRS)
At a glance
Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Amount of opioid medication used post-operatively for 14 days
Measured over 14 days post-surgery
Conditions
Where it's being run
1 sites across 1 statesCalifornia1
Study leadership
- Todd Alamin, MD · PRINCIPAL_INVESTIGATOR · Stanford University
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
Do you actually qualify for this trial?
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Eligibility criteria
Inclusion
Age 18+
Undergoing ACL reconstruction surgery at Stanford Sports Medicine Redwood City, with autograft or allograft, with or without concomitant meniscal repair.
Exclusion
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.
What this trial measures
- Amount of opioid medication used post-operatively for 14 days14 days post-surgery