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NCT04138394: VICToRY
VItamin C in Thermal injuRY: The VICToRY Trial
Phase 3 trial testing Ascorbic Acid in Shock in 666 participants. Suspended.
18 December 2025
Quick facts
| Lead sponsor | Clinical Evaluation Research Unit at Kingston General Hospital |
|---|---|
| Phase | Phase 3 |
| Status | Suspended |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | single group |
| Masking | quadruple |
| Primary purpose | treatment |
| Enrollment | 666 |
| Start date | 24 July 2020 |
| Primary completion | 18 December 2025 |
| Estimated completion | 31 March 2026 |
| Sites | 33 locations across Costa Rica, Belgium, United Kingdom, Germany, Paraguay, Mexico, Canada, Thailand |
Drugs / interventions tested
- Ascorbic Acid (ASCORBIC ACID) — full drug profile →
- placebo
Conditions studied
- Shock — all drugs for Shock →
- Thermal Burn — all drugs for Thermal Burn →
Sponsor
Clinical Evaluation Research Unit at Kingston General Hospital
Who can join
18 and older, any sex, with Shock or Thermal Burn. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
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.
Publications & conference data
5 peer-reviewed publications reference this trial (live from Europe PMC):
-
Oxidative Stress and Hyper-Inflammation as Major Drivers of Severe COVID-19 and Long COVID: Implications for the Benefit of High-Dose Intravenous Vitamin C.
Vollbracht C, Kraft K. · · 2022 · cited 97× · PMID 35571085 · DOI 10.3389/fphar.2022.899198 -
Nutritional and metabolic modulation of inflammation in critically ill patients: a narrative review of rationale, evidence and grey areas.
Rousseau AF, Martindale R. · · 2024 · cited 18× · PMID 39088114 · DOI 10.1186/s13613-024-01350-x -
Intravenous vitamin C monotherapy in critically ill patients: a systematic review and meta-analysis of randomized controlled trials with trial sequential analysis.
Lee ZY, Ortiz-Reyes L, Lew CCH, Hasan MS, et al · · 2023 · cited 16× · PMID 36882644 · DOI 10.1186/s13613-023-01116-x -
An update of the effects of vitamins D and C in critical illness.
Hill A, Starchl C, Dresen E, Stoppe C, et al · · 2022 · cited 12× · PMID 36726354 · DOI 10.3389/fmed.2022.1083760 -
[Vitamin C and D supplementation in critically ill patients].
Hill A, Starchl C, Dresen E, Stoppe C, et al · · 2023 · cited 5× · PMID 36629872 · DOI 10.1007/s00063-022-00986-6
Verify or expand the search:
- PubMed search for NCT04138394
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of Ascorbic Acid
Trials testing the same drug.
- NCT03066115 — Impact of NOS, COX, and ROS Inhibition on Cerebral Blood Flow Regulation · Phase 1 · withdrawn
- NCT04354428 — Treatment for COVID-19 in High-Risk Adult Outpatients · Phase 2, PHASE3 · terminated
- NCT04342728 — Coronavirus 2019 (COVID-19)- Using Ascorbic Acid and Zinc Supplementation · NA · completed
- NCT04328961 — Hydroxychloroquine for COVID-19 Post-exposure Prophylaxis (PEP) · Phase 2, PHASE3 · completed
- NCT04035096 — The Effectiveness of High-dose Intravenous Vitamin c With Very Low Carbohydrate Diet for Terminal Colon Cancer Patients · Phase 1, PHASE2 · unknown
Other recruiting trials for Shock
Currently open trials in the same condition.
- NCT07273643 — Characterization of Extracellular Vesicles From the Cord Blood of Extremely Preterm New Borns and Their Correlation With · recruiting
- NCT07009665 — Fluid Management and Individualized Resuscitation in Sepsis · NA · recruiting
- NCT06713668 — Augmented Pacing for Shock in the Cardiac Intensive Care Unit · NA · recruiting
- NCT06930235 — Effectiveness of Midodrine as an Adjuvant to Norepinephrine in Weaning Critically Ill Patients From Vasopressors · NA · recruiting
- NCT06920173 — Pulse Study: Peripheral Use of Low-dose Vasopressors for Safety and Efficacy in the Intensive Care Unit · Phase 2 · recruiting
Other Clinical Evaluation Research Unit at Kingston General Hospital trials
Trials by the same sponsor.
- NCT04242966 — The Effect of Higher Protein Dosing in Critically Ill Patients Ultrasound a Sub-study · Phase 3 · withdrawn
- NCT04931940 — The EFFORT Trial and EFFORT Outcomes Sub-study (EFFORT-Outcomes) · NA · unknown
- NCT05401552 — Phosphate Bioavailability Hormonal Response to a Breakfast Meal in Healthy Humans · NA · completed
- NCT03160547 — The Effect of Higher Protein Dosing in Critically Ill Patients · NA · completed
- NCT03021902 — Nutrition and Exercise in Critical Illness · Phase 2 · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT04138394 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Clinical Evaluation Research Unit at Kingston General Hospital
- Last refreshed: 6 April 2026
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04138394.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing