Does the Use of a Simplified Pain Questionnaire Impact Opioid Consumption Among People Receiving Anterior Cruciate Ligament (ACL) Knee Surgery?
Part of paid clinical trials in Redwood City, California.
- Sponsor
- Stanford University
- Study ID
- NCT07065266
- Status
- Enrolling By Invitation
Conditions
- Anterior Cruciate Ligament (ACL) Reconstruction
- Anterior Cruciate Ligament/Surgery
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Binary pain questionnaire — OTHERPost-operative questionnaire that asks if pain is 'tolerable' or 'intolerable'
- Numerical Pain Rating Scale (NPRS) — OTHERStandard 10-point pain scale used post-operatively to assess pain
Study Details
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 Dates
- Start date
- Jul 24, 2020
- Status verified
- Jul 2025
- Primary completion
- Jul 1, 2026
- Completion
- Jul 1, 2026
Study Design
- Enrollment
- 130 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- OTHER
Arms
- Active Comparator: 10-point pain scaleparticipants undergoing ACL reconstructive surgery are asked to use a 10-point NPRS pain scale to describe their pain post-operatively
- Experimental: Binary pain questionnaireParticipants undergoing ACL reconstructive surgery are asked to describe their pain as tolerable or intolerable post-operatively
Primary Outcome Measure
Amount of opioid medication used post-operatively for 14 days [ Time Frame: 14 days post-surgery ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Stanford Orthopaedic and Sports Medicine | Redwood City | California | 94063 | - |
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