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VItamin C in Thermal injuRY: The VICToRY Trial

Shock | Thermal Burn

This study aims to show that giving high dose, intravenous vitamin C in addition to standard care to burned critically ill patients will be associated with less organ dysfunction, improved survival and a quicker rate of recovery. In this study, all patients will receive standard care and of the patients will also receive high dose intravenous vitamin C, while the other half of patients will receive placebo.

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Participation Requirements

  • Sex:

    ALL
  • Eligible Ages:

    18 and up

Participation 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.

Study Location

Sunnybrook Health Sciences Centre, Ross Tilley Burn Centre
Sunnybrook Health Sciences Centre, Ross Tilley Burn Centre
Toronto, Ontario
Canada

Contact Study Team

Primary Contact

Ashley Ahuja, NP

[email protected]
416-480-6100
Hamilton General Hospital, Hamilton Health Sciences Corporation
Hamilton General Hospital, Hamilton Health Sciences Corporation
Hamilton, Ontario
Canada

Contact Study Team

Primary Contact

Diana Tedesco, RC

[email protected]
905-521-2100
Centre de recherche du CHUM
Centre de recherche du CHUM
Montréal, Quebec
Canada

Contact Study Team

Primary Contact

Cindy Prie

[email protected]
514-890-8000
Backup Contact

Maya Salame

[email protected]
514-890-8000
QEII Health Sciences Centre
QEII Health Sciences Centre
Halifax, Nova Scotia
Canada

Contact Study Team

Primary Contact

Valerie Barrette, RN

[email protected]
902∙473-7715
Study Sponsored By
Clinical Evaluation Research Unit at Kingston General Hospital
Participants Required
More Information
Study ID: NCT04138394