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A Pain and Coordination Plan for Reduced Opioid Use After Accidental Injuries

Study acronym: PAC-plan
StatusActive, Not Recruiting
PhaseNot applicable
Started
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Record History

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  1. Minor Primary completion date changed from estimate of Apr 2026 to Apr 30, 2026
    • Site details revised
    v6
  2. Minor Re-verified, no change to tracked fieldsv5
  3. Minor Trial status: Recruiting to Active, Not Recruitingv4 Show 5 more changesShow less
    • Enrollment target: estimated 232 to confirmed 271
    • Primary completion date: Sep 2026 to Apr 2026
    • Secondary endpoints: 17 to 20
    • Study description expanded, about 36 words
    • Site details revised
  4. Notable Trial status: Not Yet Recruiting to Recruiting
    • Start date: Sep 2023 to Sep 25, 2023
    • Site details revised
    v3
  5. Minor Secondary endpoints revised (17)
    • Study description expanded, about 3 words
    v2
  6. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
This clinical trial aims to lower the number of people who use opioids and improve the quality of health in patients who have experienced accidental injury by implementing a Pain and Coordination Plan (PAC-plan). The PAC-plan will be given upon discharge from the hospital. The main questions this study aims to answer are: * Can the PAC-plan reduce opioid use in patients after accidental injuries? * Can the PAC-plan increase quality of life in patients after accidental injuries? * Is implementation of the PAC-plan after accidental injuries cost-effective? Participants will be randomly assigned to the PAC-plan or usual care. The PAC-plan includes: * an opioid management plan upon discharge from the hospital * an appointment with his/her general practitioner within 2-4 weeks after discharge * the general practitioner will be given the opportunity for increased collaboration with the hospital specialists Participants in both groups will be asked to answer questionnaires about their health at discharge, and at 6 and 52 weeks after discharge from the hospital. In addition, the researchers will use data from the Norwegian Prescription Database to measure use of opioids and other relevant drugs, the Norwegian Patient Registry (NPR) and the Norwegian Registry for Primary Health Care (KPR) for the use of health care services and Statistics Norway for data on sick leave and other social security benefits.
Trial Details
NCT Number NCT06055205
Lead Sponsor University of Oslo
Collaborators: Oslo University Hospital, The Norwegian Research Fund for General Practice
Conditions
(from sponsor)
Opioid Use, Injury Traumatic, Pain, Postoperative
Related terms Agnosia, Pain, Postoperative Pain, Wounds and Injuries
Enrollment 271 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov