Impact of Counseling and Education on Opioid Consumption After ACL Reconstruction (NCT04885231) | Clinical Trial Compass
CompletedNot Applicable
Impact of Counseling and Education on Opioid Consumption After ACL Reconstruction
United States121 participantsStarted 2021-05-12
Plain-language summary
Research question: Does an opioid limiting pain management counseling and education program result in decreased opioid consumption and improved pain control compared to traditional pain management programs after anterior cruciate ligament reconstruction (ACLR) surgery?
At many institutions, the current standard of care is to instruct patients to take opioid pain medicine as needed when in severe pain to "stay ahead of the pain." This study is investigating whether modifying the instructions to take opioid pain medications only if in "unbearable pain" will have an effect on 1) reducing opioid consumption and 2) improving pain levels.
Adults who are undergoing an ACLR surgery will be invited to participate in the study and be randomly assigned to one of the two pain management programs. All patients will receive a comprehensive multi-modality pain management treatments and medications. Patients in both groups will receive the same type and amount of all postoperative medications. The only difference will be in the instructions about when to take the opioid medications.
The patients will then be sent an electronic survey twice per day for 2 weeks about their pain levels and number of opioid pills taken.
Who can participate
Age range14 Years
SexALL
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Inclusion criteria
✓. Men and women aged 14 years and older
✓. All patients scheduled to undergo an ACLR with or without concomitant procedures such as arthroscopic cartilage procedures, meniscus repair or meniscectomy, and/or lateral extraarticular tenodesis (anterolateral ligament reconstruction)
✓. Willing to participate in a perioperative pain management education and counseling program
✓. Willing to track pain levels and opioid consumption through surveys administered via text
✓. Willing to receive a perioperative regional nerve block
✓. Language skills and cognitive ability required to participate in the study
✓. Provision of informed consent
Exclusion criteria
✕. Revision ACLR
✕. Concomitant open cartilage procedures or additional knee ligament repair or reconstruction