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Study identifier: NCT06949826 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Buprenorphine as a Post-operative Analgesic in Opioid-Naive Patients After Ankle Fracture Surgery

Condition: Pain, Postoperative · Ankle Fracture Surgery · Opioid Use Disorder  ·  Sponsor: Jenna-Leigh Wilson

PhasePhase 4
Planned participants100
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Addictive full-agonist opioids, like oxycodone and hydrocodone, are often used to treat pain after surgery. However, these full-agonist opioids can be very addictive. After ankle fracture surgery, about 1 in 5 patients that did not take opioids before surgery become addicted to opioids after surgery. Buprenorphine is an opioid with unique properties that may offer a way to reduce the number of patients that become addicted to opioids after surgery. Buprenorphine has good analgesic (painkilling) effects. It is also thought to be less addictive and cause less of a high than full-agonist opioids, like oxycodone and hydrocodone. This project's goal is to determine if transdermal buprenorphine can safely and effectively control pain after ankle fracture surgery. This study will be a pilot study, which sets the stage for future studies that investigate whether buprenorphine can reduce the rate that patients become addicted to opioids after surgery. This study's multidisciplinary team will divide patients into two groups. Participants in one group will be treated with a 7-day transdermal buprenorphine patch (where the buprenorphine is slowly absorbed through the skin over 7 days). Participants in the other group will be treated with a placebo patch. A placebo has no drug in it, it just looks like the buprenorphine patch. Aside from the buprenorphine patch or placebo patch, both groups' pain management plans will be the same as if they were not in the study. Over the first week after…

This description comes directly from the study's public registry record.

Talk to the study team

Noah J Harrison, MD, MMSc  ·  314-459-1140  ·  nharrison@wustl.edu

Juanita Taylor, MPA, BS, RRT  ·  314-454-7047  ·  jrtaylor@wustl.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Washington University in St. Louis/Barnes Jewish HospitalSt Louis, Missouri, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06949826