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 — OTHER
    Post-operative questionnaire that asks if pain is 'tolerable' or 'intolerable'
  • Numerical Pain Rating Scale (NPRS) — OTHER
    Standard 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 scale
    participants undergoing ACL reconstructive surgery are asked to use a 10-point NPRS pain scale to describe their pain post-operatively
  • Experimental: Binary pain questionnaire
    Participants 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)

FacilityCityStateZIPSite coordinators
Stanford Orthopaedic and Sports MedicineRedwood CityCalifornia94063-

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