NCT04970069
Completed
Not Applicable
The Effect of Preoperative Education on Postoperative Opioid Consumption
ConditionsPostoperative Pain
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Postoperative Pain
- Sponsor
- The Cleveland Clinic
- Enrollment
- 1057
- Locations
- 1
- Primary Endpoint
- Opioid Consumption
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
The investigators will evaluate the effect of preoperative education on postoperative opioid.
Detailed Description
The investigators propose a randomized trial to be performed at the Cleveland Clinic. Patients will be assigned to: 1) an educational video focused on postoperative analgesia modalities, opioids, and realistic pain expectations (analgesic education); or, 2) an educational video focused on other aspects of the perioperative experience.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Modified informed consent
- •Adults ≥18 years
- •American Society of Anaesthesiologists physical status 1-4
- •Scheduled for hip arthroplasty, laparoscopy assisted colorectal surgery
- •Personal visit the PACE clinic
- •Anticipated overnight postoperative hospitalization
- •Reasonable English fluency
Exclusion Criteria
- •Opioid use for more than 30 consecutive days within three preoperative months, at a daily dose of 15 mg or more of morphine or equivalent
- •Regional block or epidural analgesia
Outcomes
Primary Outcomes
Opioid Consumption
Time Frame: 72 hours after surgery
Opioid consumption (morphine milligrams equivalent) during the initial 72 hours after surgery.
Secondary Outcomes
- Time-weighted Average Pain Scores(72 hours after surgery, or until discharge, whichever was earlier)
- Satisfaction With Post Operative Pain Management(3 days after surgery)
Study Sites (1)
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