ClinConnect ClinConnect Logo
Search / Trial NCT04138394

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.

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

0 patients applied

Trial Officials

Daren K Heyland, MD

Principal Investigator

Queen's University

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Similar Trials