VItamin C in Thermal injuRY: The VICToRY Trial
Launched by CLINICAL EVALUATION RESEARCH UNIT AT KINGSTON GENERAL HOSPITAL · Oct 22, 2019
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
The VICToRY Trial is a clinical study looking at the effects of high doses of intravenous vitamin C on critically ill patients with serious burn injuries. The goal is to see if giving vitamin C, along with standard medical care, can help these patients recover faster, have better organ function, and improve their chances of survival compared to those who do not receive vitamin C. In this trial, half of the participants will receive the vitamin, while the other half will receive a placebo, which is a harmless substance that looks like the treatment but has no active ingredients.
To be eligible for the trial, participants must be at least 18 years old and have deep burns that cover at least 20% of their body, requiring skin grafting. However, certain individuals, such as those who are pregnant, have specific health conditions, or are already receiving vitamin C treatments, will not be able to participate. If you or someone you know is interested in this study, it’s important to discuss this with a healthcare provider to see if it’s a good fit. Participants can expect to receive standard care for their burns, along with either the vitamin C treatment or the placebo, and their health will be closely monitored throughout the study.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 18 years of age or older
- • Deep 2nd and/or 3rd degree burns requiring skin grafting
- • Minimum burn size of ≥ 20% Total Body Surface Area (TBSA)
- Exclusion Criteria:
- • \>24 hours from admission to participating hospital to consent.
- • Patients admitted to burn unit \>24 from injury or accident.
- • Patients who are moribund (not expected to survive the next 72 hours).
- • Pregnancy (pregnancy will be ruled out as part of standard of care) or lactating.
- • Enrollment in another industry sponsored ICU intervention study.
- • Receiving high-dose IV vitamin C already (enteral or oral vitamin C is allowed).
- • Known glucose-6-phosphate dehydrogenase (G6PD) deficiency.
- • Recent history of kidney stones (within the last year).
- • Concomitant use of hydroxycobalamin (vitamin B12) for suspected cyanide poisoning.
About Clinical Evaluation Research Unit At Kingston General Hospital
The Clinical Evaluation Research Unit at Kingston General Hospital is dedicated to advancing medical knowledge and patient care through rigorous clinical research. This unit specializes in the design, implementation, and analysis of clinical trials across various therapeutic areas, aiming to evaluate the efficacy and safety of innovative treatments and interventions. With a commitment to ethical standards and patient-centered research, the unit collaborates with healthcare professionals, academic institutions, and industry partners to foster a robust research environment that enhances clinical practice and improves health outcomes in the community.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Bridgeport, Connecticut, United States
Washington, District Of Columbia, United States
Bangkok, , Thailand
Iowa City, Iowa, United States
Chicago, Illinois, United States
Saint Louis, Missouri, United States
Houston, Texas, United States
San Luis Potosí, , Mexico
Würzburg, , Germany
Liège, , Belgium
Wakefield, , United Kingdom
Montréal, Quebec, Canada
Chelsea, London, United Kingdom
Ghent, Oost Vlaanderen, Belgium
Birmingham, , United Kingdom
Phoenix, Arizona, United States
Tampa, Florida, United States
Augusta, Georgia, United States
Ohio City, Ohio, United States
Dallas, Texas, United States
Seattle, Washington, United States
Brussels, , Belgium
Toronto, Ontario, Canada
Québec, , Canada
Aachen, , Germany
Cologne, , Germany
Ludwigshafen, , Germany
Asunción, , Paraguay
Prescot, , United Kingdom
San José, , Costa Rica
Charleroi, Hainaut, Belgium
Hamilton, Ontario, Canada
Milwaukee, Wisconsin, United States
Halifax, Nova Scotia, Canada
Québec, , Canada
Dallas, Texas, United States
Tübingen, Baden Württemberg, Germany
Leipzig, Saxonia, Germany
Cologne, , Germany
Tübingen, , Germany
Patients applied
Trial Officials
Daren K Heyland, MD
Principal Investigator
Queen's University
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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