Pain, AcuteNCT05555576
Impact of Vitamin C on opioïd Consumption After an Emergency Department Visit for Acute Musculoskeletal Pain
A study testing Vitamin C in people with Pain, Acute, run by Centre Integre Universitaire de Sante et Services Sociaux du Nord de l'ile de Montreal at 1 site in Canada.
Trial summary
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… Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Pain, Acute
- What is being tested?
- Vitamin C
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 464 participants
- Where
- 1 siteCanada
- Study dates
- 1 Nov 2023to Dec 2026
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Aged 18 and over;
- Treated in ED for acute musculoskeletal pain present for less than 2 weeks;
- Discharged with an opioid prescription;
- Speaks French or English.
Who cannot join
- Opioid use 1 month prior to the ED visit;
- Already taking vitamin C supplement;
- Active cancer;
- Treated for chronic pain;
- Treated for opioid use disorder;
- Unable to fill out diary or unavailable for follow-up;
Show all 9Show fewer
- Any allergy, intolerance or sensitivity to milk (lactose) or morphine
- Treated with cyclosporin or coumadin
- Pregnant or lactating (dosage > 1,800 mg not recommended. For women of child-bearing age and sexually active in the past 3 months, a urine pregnancy test will be performed.)
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Impact of Vitamin C on the Reduction of Opioid Consumption After an Emergency Department Visit for Acute Musculoskeletal Pain: A Double-Blind Randomized Control Trial Protocol
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.
Read the detailed description
Study Rationale Literature suggests that the administration of vitamin C has an effect in reducing pain and opioid consumption in the context of immediate postoperative acute pain. However, the investigators could not find evidence on the effectiveness of vitamin C administration after an ED visit in the context of acute pain, notably in trauma injuries like fractures, bruises, sprains, strains, etc. Previous studies have only evaluated pain relief and opioid use for the immediate postoperative period of 24 to 72 hours. Therefore, the investigators propose to evaluate the efficacy of a 14-day regiment of vitamin C given to ED patients discharged with an opioid prescription for acute musculoskeletal (MSK) pain on total opioid consumption after two weeks. The two-week period was chosen because it defines the usual acute pain time frame, during which need for analgesics including opioids is essentially resolved in most patients (88% of our previous study cohort). Furthermore, since vitamin C is also associated with less post-herpetic neuralgia and complex regional pain syndromes (CRPS), the investigators also propose to evaluate its impact on the incidence of chronic pain and CRPS at 3 months.
Study Objectives The primary aim is to compare the difference in the total morphine 5 mg equivalent pills consumed after a two-week follow-up between patients receiving vitamin C versus patients receiving a placebo during these two weeks.
The secondary aims are to compare the following between patients receiving vitamin C vs patients receiving a placebo: pain intensity trajectories, average pain relief during the two-week, side effects, total morphine 5 mg equivalent pills consumed after a two-week follow-up for each type of MSK pain (fracture, contusions, cervical pain, lower back pain, MSK pain at other sites), incidence of chronic pain (including CRPS) at 3 months globally and for each type of MSK pain, incidence of CRPS for limb fractures, and for a wrist fracture in particular at 3 months, and prevalence of opioid use at 3 months.
Study Design The investigators will conduct a multi-center, double-blind, randomized, placebo-controlled trial performed in two tertiary trauma care university-affiliated hospitals located in Montreal and in Quebec City (Quebec, Canada) with an annual census of 60,000 and 67,000 visits, respectively.
Participants and recruitment Consecutive patients (from 8 to 20h every day) diagnosed with an acute musculoskeletal pain complaint ongoing for less than two weeks and discharged from the ED with an opioid prescription will be approached by the treating clinician to participate in the study and obtain their verbal consent to be seen by a research assistant. The decision to prescribe opioids will be at the discretion of the treating physician, but included patients will receive a standardized prescription of 20 pills of morphine 5 mg based on our previous work. The research assistant will then verify the patient's inclusion and exclusion criteria, explain the research protocol, and obtain informed written consent. Patients will be assessed via a two-week electronic (or paper) diary and contacted 3 months after ED discharge.
Randomization method and blinding Eligible patients will be block randomized at the initial visit (via 1:1 ratio) to either 1 000 mg vitamin C taken orally twice a day or matching placebo, using a centralized randomisation web system. Allocation concealment will be in place to ensure that the investigator and the individual enrolling the subject into the study have no prior knowledge of group assignment. Since fractures are associated with more opioid consumption, randomization will be a stratified by fracture or not and centre. According to the centralized web system, an independent pharmacist will dispense pre-packed numbered bottles of either vitamin C or placebo capsules for each patient. Both will be dispensed an identical capsules and the pharmacist will be unaware of the trial-group assignments. Each participant will be assigned a number and received the capsules in the corresponding pre-packed bottle. Group allocation will be disclosed only after final analysis or at the request of the patient's treating clinician.
Study drug Vitamin C (ascorbic acid) is a vital nutrient; it helps form and maintain bones, skin, and blood vessels and has antioxidant properties. It is not produced by the human body but occurs naturally in fruits and vegetables and other foods. It is also available as supplement over the counter in pharmacies, supermarkets, and health supplements stores and online. For adults, the recommended daily amount of vitamin C is 65 to 90 milligrams (mg) a day (Recommended Dietary Allowances by the Government of Canada).
- Conditions
- Pain, Acute
- Being tested
- Vitamin C, Placebo
- Keywords
- Vitamin C, Opioids, Emergency department, Pain
- Medical subject headings
- Acute Pain, Emergencies, Pain
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Vitamin CDietary supplement
1000 mg vitamin C taken orally twice a day (one in the morning and one in the evening) for a 14-day period after ED discharge for the treatment arm
PlaceboOther
Placebo taken orally twice a day (one in the morning and one in the evening) for a 14-day period after ED discharge for the treatment arm
| Study group | Role | What they receive |
|---|---|---|
| Vitamin C | Experimental | 1 000 mg vitamin C taken orally twice a day Receives: Dietary Supplement: Vitamin C |
| Placebo | Placebo comparator | Matching placebo Receives: Other: Placebo |
What is being measured
The primary outcome is the main question the study is designed to answer.
Difference in the total morphine 5 mg equivalent pills consumed
Compare the difference in the total morphine 5 mg equivalent pills consumed after a two-week follow-up between patients receiving vitamin C versus patients receiving a placebo during these two weeks.
Measured: 14 days
Secondary outcomes (7)
Pain intensity trajectories
Compare pain intensity trajectories, measured on an 11-point numerical rating scale (NRS) from 0 to 10 (0 is no pain and 10 worst pain imaginable), between both groups with group-based trajectory modelling.
Measured: 14 days
Average pain relief
Patient's average pain relief during the two-week, measured on an 11-point numerical rating scale (NRS) from 0 to 10 (0 is no pain and 10 worst pain imaginable).
Measured: 14 days
Number (%) of participants with side effects
Patients will report which of the following side effects were experienced during the 14-day period: nausea, vomiting, constipation, dizziness, drowsiness, sweating, weakness, or other side effects.
Measured: 14 days
Total morphine 5 mg equivalent pills consumed for each type of musculoskeletal (MSK) pain
Fracture, contusions, cervical pain, lower back pain, MSK pain at other sites
Measured: 14 days
Incidence of chronic pain (including complex regional pain syndrome (CRPS)) globally and for each type of MSK pain
Globally and for each type of MSK pain using pain disability index (PDI) or Budapest criteria
Measured: 3 months
Incidence of CRPS for limb fractures, and for a wrist fracture
For these cases in particular using Budapest criteria
Measured: 3 months
Prevalence of opioid use
Patients will be asked if they still consumed opioids at 3 months
Measured: 3 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted27 Sep 2022
- Study start1 Nov 2023
- Primary completion20 Jun 2026
- Study completionDec 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (2)Papers the sponsor has linked to this study.
- Other trials for Pain, AcuteStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Basic science
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Double-blind randomized placebo-controlled trial
- Masking
- Triple blind
- Who is masked
- Participant, Care provider, Investigator
- Enrolment
- 464 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Centre Integre Universitaire de Sante et Services Sociaux du Nord de l'ile de Montreal
- Sponsor type
- University, hospital or other
- Collaborators
- Hopital de l'Enfant-Jesus
- Responsible party
- Principal investigator, Raoul Daoust, Centre Integre Universitaire de Sante et Services Sociaux du Nord de l'ile de Montreal
- Investigators
- Raoul Daoust, MD MSc, Principal investigator, Université de Montréal
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05555576
- Sponsor's protocol ID
- 2023-2442
- Status last verified
- Oct 2026
- First submitted
- 20 Sep 2022
- Last updated
- 26 Oct 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Daoust R, Paquet J, Williamson D, Huard V, Arbour C, Perry JJ, Emond M, Berthelot S, Archambault P, Rouleau D, Morris J, Cournoyer A. Impact of vitamin C on the reduction of opioid consumption for acute musculoskeletal pain: A double-blind randomized control pilot study. PLoS One. 2024 Dec 31;19(12):e0316450. doi: 10.1371/journal.pone.0316450. eCollection 2024.
PubMed 39739762Daoust R, Paquet J, Chauny JM, Williamson D, Huard V, Arbour C, Emond M, Rouleau D, Cournoyer A. Impact of vitamin C on the reduction of opioid consumption after an emergency department visit for acute musculoskeletal pain: a double-blind randomised control trial protocol. BMJ Open. 2023 May 24;13(5):e069230. doi: 10.1136/bmjopen-2022-069230.
PubMed 37225265
Study at a glance
From the registry record, last updated by the sponsor on 26 Oct 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Impact of Vitamin C on the Reduction of Opioid Consumption After an Emergency Department Visit for Acute Musculoskeletal Pain: A Double-Blind Randomized Control Trial Protocol
- ClinicalTrials.gov ID
- NCT05555576
- Acronym / sponsor ID
- 2023-2442
- Conditions
- Pain, Acute
- Keywords
- Vitamin C, Opioids, Emergency department, Pain
- Study type
- Interventional
- Recruitment status
- Active, not recruiting
- Enrolment
- 464 participants (estimated)
- Lead sponsor
- Centre Integre Universitaire de Sante et Services Sociaux du Nord de l'ile de MontrealUniversity, hospital or other
- Collaborators
- Hopital de l'Enfant-Jesus
- Study start
- 1 Nov 2023 (actual)
- Primary completion
- 20 Jun 2026 (actual)
- Study completion
- Dec 2026 (estimated)
- First posted
- 27 Sep 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Detailed description
Study Rationale Literature suggests that the administration of vitamin C has an effect in reducing pain and opioid consumption in the context of immediate postoperative acute pain. However, the investigators could not find evidence on the effectiveness of vitamin C administration after an ED visit in the context of acute pain, notably in trauma injuries like fractures, bruises, sprains, strains, etc. Previous studies have only evaluated pain relief and opioid use for the immediate postoperative period of 24 to 72 hours. Therefore, the investigators propose to evaluate the efficacy of a 14-day regiment of vitamin C given to ED patients discharged with an opioid prescription for acute musculoskeletal (MSK) pain on total opioid consumption after two weeks. The two-week period was chosen because it defines the usual acute pain time frame, during which need for analgesics including opioids is essentially resolved in most patients (88% of our previous study cohort). Furthermore, since vitamin C is also associated with less post-herpetic neuralgia and complex regional pain syndromes (CRPS), the investigators also propose to evaluate its impact on the incidence of chronic pain and CRPS at 3 months.
Study Objectives The primary aim is to compare the difference in the total morphine 5 mg equivalent pills consumed after a two-week follow-up between patients receiving vitamin C versus patients receiving a placebo during these two weeks.
The secondary aims are to compare the following between patients receiving vitamin C vs patients receiving a placebo: pain intensity trajectories, average pain relief during the two-week, side effects, total morphine 5 mg equivalent pills consumed after a two-week follow-up for each type of MSK pain (fracture, contusions, cervical pain, lower back pain, MSK pain at other sites), incidence of chronic pain (including CRPS) at 3 months globally and for each type of MSK pain, incidence of CRPS for limb fractures, and for a wrist fracture in particular at 3 months, and prevalence of opioid use at 3 months.
Study Design The investigators will conduct a multi-center, double-blind, randomized, placebo-controlled trial performed in two tertiary trauma care university-affiliated hospitals located in Montreal and in Quebec City (Quebec, Canada) with an annual census of 60,000 and 67,000 visits, respectively.
Participants and recruitment Consecutive patients (from 8 to 20h every day) diagnosed with an acute musculoskeletal pain complaint ongoing for less than two weeks and discharged from the ED with an opioid prescription will be approached by the treating clinician to participate in the study and obtain their verbal consent to be seen by a research assistant. The decision to prescribe opioids will be at the discretion of the treating physician, but included patients will receive a standardized prescription of 20 pills of morphine 5 mg based on our previous work. The research assistant will then verify the patient's inclusion and exclusion criteria, explain the research protocol, and obtain informed written consent. Patients will be assessed via a two-week electronic (or paper) diary and contacted 3 months after ED discharge.
Randomization method and blinding Eligible patients will be block randomized at the initial visit (via 1:1 ratio) to either 1 000 mg vitamin C taken orally twice a day or matching placebo, using a centralized randomisation web system. Allocation concealment will be in place to ensure that the investigator and the individual enrolling the subject into the study have no prior knowledge of group assignment. Since fractures are associated with more opioid consumption, randomization will be a stratified by fracture or not and centre. According to the centralized web system, an independent pharmacist will dispense pre-packed numbered bottles of either vitamin C or placebo capsules for each patient. Both will be dispensed an identical capsules and the pharmacist will be unaware of the trial-group assignments. Each participant will be assigned a number and received the capsules in the corresponding pre-packed bottle. Group allocation will be disclosed only after final analysis or at the request of the patient's treating clinician.
Study drug Vitamin C (ascorbic acid) is a vital nutrient; it helps form and maintain bones, skin, and blood vessels and has antioxidant properties. It is not produced by the human body but occurs naturally in fruits and vegetables and other foods. It is also available as supplement over the counter in pharmacies, supermarkets, and health supplements stores and online. For adults, the recommended daily amount of vitamin C is 65 to 90 milligrams (mg) a day (Recommended Dietary Allowances by the Government of Canada).
Study design
- Primary purpose
- Basic science
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind (participant, care provider, investigator)
- Number of arms
- 2
- Model description
- Double-blind randomized placebo-controlled trial
| Arm | Type | Receives |
|---|---|---|
| Vitamin C | Experimental | Dietary Supplement: Vitamin C1 000 mg vitamin C taken orally twice a day |
| Placebo | Placebo comparator | Other: PlaceboMatching placebo |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- Aged 18 and over;
- Treated in ED for acute musculoskeletal pain present for less than 2 weeks;
- Discharged with an opioid prescription;
- Speaks French or English.
Key exclusion criteria (9 listed)
- Opioid use 1 month prior to the ED visit;
- Already taking vitamin C supplement;
- Active cancer;
- Treated for chronic pain;
- Treated for opioid use disorder;
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Vitamin C1000 mg vitamin C taken orally twice a day (one in the morning and one in the evening) for a 14-day period after ED discharge for the treatment arm | Dietary supplement | Vitamin C |
| PlaceboPlacebo taken orally twice a day (one in the morning and one in the evening) for a 14-day period after ED discharge for the treatment arm | Other | Placebo |
Primary outcome
Difference in the total morphine 5 mg equivalent pills consumed
Time frame: 14 days
Compare the difference in the total morphine 5 mg equivalent pills consumed after a two-week follow-up between patients receiving vitamin C versus patients receiving a placebo during these two weeks.
7 secondary outcomes
Pain intensity trajectories
Time frame: 14 days
Average pain relief
Time frame: 14 days
Number (%) of participants with side effects
Time frame: 14 days
Total morphine 5 mg equivalent pills consumed for each type of musculoskeletal (MSK) pain
Time frame: 14 days
Incidence of chronic pain (including complex regional pain syndrome (CRPS)) globally and for each type of MSK pain
Time frame: 3 months
Incidence of CRPS for limb fractures, and for a wrist fracture
Time frame: 3 months
Prevalence of opioid use
Time frame: 3 months
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 26 Oct 2026.
- Derived from this study: PubMed 39739762Daoust R, Paquet J, Williamson D, Huard V, Arbour C, Perry JJ, Emond M, Berthelot S, Archambault P, Rouleau D, Morris J, Cournoyer A. Impact of vitamin C on the reduction of opioid consumption for acute musculoskeletal pain: A double-blind randomized control pilot study. PLoS One. 2024 Dec 31;19(12):e0316450. doi: 10.1371/journal.pone.0316450. eCollection 2024.
- Derived from this study: PubMed 37225265Daoust R, Paquet J, Chauny JM, Williamson D, Huard V, Arbour C, Emond M, Rouleau D, Cournoyer A. Impact of vitamin C on the reduction of opioid consumption after an emergency department visit for acute musculoskeletal pain: a double-blind randomised control trial protocol. BMJ Open. 2023 May 24;13(5):e069230. doi: 10.1136/bmjopen-2022-069230.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Raoul Daoust, MD MSc principal investigator
Université de Montréal
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Vitamin C in people with Pain, Acute, run by Centre Integre Universitaire de Sante et Services Sociaux du Nord de l'ile de Montreal at 1 site in Canada.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: under way, not looking for participants, as of the sponsor's last update on 26 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Difference in the total morphine 5 mg equivalent pills consumed (time frame: 14 days). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT05555576, which also lists 2 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Oct 2026.