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N/A N=1,057 Randomized Double-blind Prevention

Preoperative Education

Postoperative Pain

Enrolled (actual)
1,057
Serious AEs
0.0%
Results posted
Jul 2024
Primary outcome: Primary: Opioid Consumption — 23; 26 Morphine milligrams equivalent — p=0.890

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Video on analgesic education (Other); Video on general perioperative education (Other)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
The Cleveland Clinic
Primary completion
Sep 2023

Outcome Measures

OutcomeResultp-value
PRIMARY
Opioid Consumption
23; 26 0.890
SECONDARY
Time-weighted Average Pain Scores
4; 4 0.617
SECONDARY
Satisfaction With Post Operative Pain Management
9; 10 0.611

Summary

The investigators will evaluate the effect of preoperative education on postoperative opioid.

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
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04970069). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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