Buprenorphine + Oxycodone for Acute Pain

(EASE Trial)

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Overseen ByD'Ann B Hershel, MS
Age: 18+
Sex: Any
Trial Phase: Phase 4
Sponsor: Wake Forest University Health Sciences
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

Traumatic injury is responsible for over 25 million (16%) Emergency Department visits and over 225,000 deaths each year per 2021 Center for Disease Control data. This is the 3rd leading cause of death in the US. Often, acute care for the injured patient requires administration of pain medication for the purposes of acute pain control from injury. The mainstay of treatment for pain control has historically involved opioid pain medication.

Who Is on the Research Team?

MP

Matthew Painter, MD, FACS

Principal Investigator

Wake Forest University Health Sciences

Are You a Good Fit for This Trial?

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive either buprenorphine or oxycodone as part of a multimodal pain control regimen

2 weeks
Daily monitoring during hospital stay

Follow-up

Participants are monitored for safety and effectiveness after treatment, including pain scores and opiate use

2 weeks
1 visit (in-person), additional virtual check-ins

What Are the Treatments Tested in This Trial?

Interventions

  • Buprenorphine
  • Oxycodone

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Group I: Study groupExperimental Treatment1 Intervention
Group II: Control groupExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Wake Forest University Health Sciences

Lead Sponsor

Trials
1,432
Recruited
2,506,000+