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Clinical Trials/NCT07065266
NCT07065266Enrolling By InvitationNot Applicable

The Utility of a Dichotomous Pain Scale in Reducing Postoperative Opioids Consumption in Outpatient ACL Surgery: A Prospective Randomized Controlled Study

Stanford University1 site in 1 country130 target enrollmentStarted: July 24, 2020Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Enrolling By Invitation
Enrollment
130
Locations
1
Primary Endpoint
Amount of opioid medication used post-operatively for 14 days

Study Overview

Brief Summary

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Undergoing ACL reconstruction surgery at Stanford Sports Medicine Redwood City, with autograft or allograft, with or without concomitant meniscal repair.

Exclusion Criteria

  • •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.

Arms & Interventions

10-point pain scale

Active Comparator

participants undergoing ACL reconstructive surgery are asked to use a 10-point NPRS pain scale to describe their pain post-operatively

Intervention: Numerical Pain Rating Scale (NPRS) (Other)

Binary pain questionnaire

Experimental

Participants undergoing ACL reconstructive surgery are asked to describe their pain as tolerable or intolerable post-operatively

Intervention: Binary pain questionnaire (Other)

Outcomes

Primary Outcomes

Amount of opioid medication used post-operatively for 14 days

Time Frame: 14 days post-surgery

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Todd Alamin

Professor of Orthopaedic Surgery

Stanford University

Study Sites (1)

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