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NCT05593341 · ClinicalTrials.gov registry record · NA
Opioid Education in Total Knee Arthroplasty
A NA study of Postoperative Pain and Opioid Use, sponsored by Hospital for Special Surgery, New York.
- Completed
- Registry status
- NA
- Development phase
- 42
- Enrollment target
- 1
- Study location
NCT05593341: Completed NA study of Postoperative Pain and Opioid Use, sponsored by Hospital for Special Surgery, New York.
NCT05593341 is a NA study of Postoperative Pain and Opioid Use that has completed, run by Hospital for Special Surgery, New York. The registered enrollment target is 42 participants, below the 231-participant average among 120 other Postoperative Pain trials with a reported enrollment target (82% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05593341, a NA study of Postoperative Pain and Opioid Use, has completed, sponsored by Hospital for Special Surgery, New York.
- COMPLETED
- Registry status
- NA
- Development phase
- 42 participants
- Enrollment target
- 1
- Study location
Study Summary
The goal of this experimental study is to compare different education intervention on opioid education for patients undergoing total knee arthroplasty. The specific research questions to address are: 1. Does perioperative education pathway reduce opioid refill requests? 2. Is education pathway that focuses on pain management provided in-person and via video in repeated sessions more effective than current standard of care education consisting of a single exposure given as part of a broader preoperative presentation covering multiple topics? 3. Is there a difference between education provided in-person vs video? 4. Does perioperative education improve compliance with multimodal analgesia? 5. Does perioperative education improve appropriate opioid storage? 6. Does perioperative education improve appropriate opioid disposal? Enrolled patients will be assigned at random to one of 3 study groups. Group 1 (control): Patients are referred to the hospital's standard 1-hour virtual patient education webinar prior to surgery. Group 2 (in-person): Patients will receive two in-person education sessions (1st session before surgery and 2nd session after surgery). Patients will also receive portable document format (pdf) handouts about opioid and pain management. Group 3 (video): Patients will receive two video education sessions (1st session before surgery and 2nd session after surgery). Patients will also receive pdf handouts about opioid and pain management.
Primary Outcome
Patients will be asked if they have refilled their opioid prescription and the number of opioid refills.
Conditions Studied
Interventions
- OTHER Opioid education in person
- OTHER Opioid education via video
Study Locations (1)
New York
- Hospital for Special Surgery - New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 42 participants |
| Start Date | 2022-09-27 |
| Est. Completion | 2023-09-11 |
| Phase | NA |
What the finished NCT05593341 record still lists
NCT05593341 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 42 participants, a relatively small participant target, below the 231-participant average among 120 other Postoperative Pain trials with a reported enrollment target (82% lower).
The record links to 5 conditions, with Postoperative Pain appearing as the primary indexed condition, and to 2 interventions - of which Opioid education in person is the first listed.
NCT05593341 reports a single indexed study location in New York.
Frequently Asked Questions
What is clinical trial NCT05593341 about?
NCT05593341 is a clinical study titled "Opioid Education in Total Knee Arthroplasty". The goal of this experimental study is to compare different education intervention on opioid education for patients undergoing total knee arthroplasty. The specific research questions to address are: 1. Does perioperative education pathway reduce opioid refill requests? 2. Is education pathway that...
What is the current status of trial NCT05593341?
This trial is currently completed. It is a NA study. The enrollment target is 42 participants. The study started on 2022-09-27. Estimated completion is 2023-09-11.
What conditions does trial NCT05593341 study?
This clinical trial studies the following conditions: Postoperative Pain, Opioid Use, Opioid Misuse, Opioid Abuse, Arthropathy of Knee.
What interventions are being tested in trial NCT05593341?
The interventions under investigation include: Opioid education in person (OTHER), Opioid education via video (OTHER).
Who is sponsoring clinical trial NCT05593341?
This trial is sponsored by Hospital for Special Surgery, New York, which has 194 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05593341 being conducted?
This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Where NCT05593341's enrollment target sits among peer trials
42 107th of 120 higher than 14 of 120 other Postoperative Pain trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Postoperative Pain trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
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