Preoperative Education
The Effect of Preoperative Education on Postoperative Opioid Consumption
1 other identifier
interventional
1,057
1 country
1
Brief Summary
The investigators will evaluate the effect of preoperative education on postoperative opioid.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable postoperative-pain
Started Jul 2021
Longer than P75 for not_applicable postoperative-pain
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 16, 2021
CompletedFirst Posted
Study publicly available on registry
July 21, 2021
CompletedStudy Start
First participant enrolled
July 25, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 15, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
September 15, 2023
CompletedResults Posted
Study results publicly available
July 25, 2024
CompletedJuly 25, 2024
July 1, 2024
2.1 years
July 16, 2021
June 7, 2024
July 9, 2024
Conditions
Outcome Measures
Primary Outcomes (1)
Opioid Consumption
Opioid consumption (morphine milligrams equivalent) during the initial 72 hours after surgery.
72 hours after surgery
Secondary Outcomes (2)
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 Arms (2)
Analgesic education
ACTIVE COMPARATORGeneral perioperative education
PLACEBO COMPARATORInterventions
A four minute video informing the patient about opioids.
A four minute video informing the patient about general perioperative process.
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Cleveland Clinic
Cleveland, Ohio, 44195, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Results Point of Contact
- Title
- Dr. Alparslan Turan
- Organization
- Cleveland Clinic
Study Officials
- PRINCIPAL INVESTIGATOR
Alparslan Turan, MD
The Cleveland Clinic
Publication Agreements
- PI is Sponsor Employee
- Yes
- Restrictive Agreement
- No
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 16, 2021
First Posted
July 21, 2021
Study Start
July 25, 2021
Primary Completion
September 15, 2023
Study Completion
September 15, 2023
Last Updated
July 25, 2024
Results First Posted
July 25, 2024
Record last verified: 2024-07