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Impact of Vitamin C on opioïd Consumption After an Emergency Department Visit for Acute Musculoskeletal Pain

StatusRecruiting
PhaseNot applicable
Started
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Record status
This record was last updated March 31, 2026 (before its estimated June 2026 completion). Its status may not reflect the trial's current state.

Record History

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  1. Minor Re-verified, no change to tracked fieldsv7
  2. Notable Primary completion date: Jun 2025 to Jun 2026
    • Study completion date: Dec 2025 to Dec 2026
    v6
  3. Notable Trial status: Not Yet Recruiting to Recruiting
    • Study sites: 0 to 1
    • Start date changed from estimate of Jan 2024 to Nov 1, 2023
    • Study title revised
    v5
  4. Notable Start date: Apr 2023 to Jan 2024
    • Primary completion date: Dec 2024 to Jun 2025
    • Study completion date: Jun 2025 to Dec 2025
    v4
  5. Notable Primary completion date: Dec 2023 to Dec 2024
    • Start date: Dec 2022 to Apr 2023
    • Study completion date: Jun 2024 to Jun 2025
    v3
  6. Minor Interventions: Vitamin C (Dietary Supplement) to Placebo (Other), Vitamin C (Dietary Supplement)v2
  7. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
Recent evidence has shown that vitamin C has some analgesic properties and can therefore reduce opioids used during healing. Vitamin C analgesic effect has been explored mostly during the short-term postoperative context or in disease specific chronic pain prevention but not after acute musculoskeletal injuries, which are often seen in the emergency department (ED). The study's primary aim is to compare the total morphine 5 mg equivalent pills consumed during a two-week follow-up between patients receiving vitamin C or a placebo after ED discharge for an acute musculoskeletal pain complaint. The investigators will conduct a double-blind randomized placebo-controlled trial with 464 participants distributed in two arms, one group receiving 1 000 mg of vitamin C twice a day for 14 days and another one receiving a placebo. Participants will be ≥18 years of age, treated in ED for acute musculoskeletal pain present for less than 2 weeks, and discharged with an opioid prescription for home pain management. Total morphine 5 mg equivalent pills consumed during the two-week follow-up will be assessed via an electronic (or paper) diary. In addition, patients will report their daily pain intensity, pain relief, side effects, and other types of pain medication or other non-pharmacological approach (ice, heat, immobilization, etc.) used. Three months after the injury, participants will also be contacted to evaluate chronic pain development. The investigators hypothesized that vitamin C, compared to a placebo, will reduce opioid consumption during a 14-day follow-up for ED discharged patients treated for acute pain.
Trial Details
NCT Number NCT05555576
Lead Sponsor Centre Integre Universitaire de Sante et Services Sociaux du Nord de l'ile de Montreal
Collaborators: Hopital de l'Enfant-Jesus
Conditions
(from sponsor)
Pain, Acute
Related terms Acute Pain, Emergencies, Pain
Enrollment 464 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov