Table 1.
Trial name | Centers | Location | #of Subjects | Study design | Entry diagnosis | Primary outcome | Trial identifier |
---|---|---|---|---|---|---|---|
Ascorbic acid, Corticosteroids, and Thiamine in Sepsis (ACTS) Trial | Multicenter | US | 200 (C) | Randomized, double-blind, placebo-controlled trial | Sepsis/septic shock | Change in Sequential Organ Failure Assessment (SOFA) score at 72 hours | NCT03389555 |
Vitamin C, Thiamine and Steroids in Sepsis (VICTAS) | Multicenter | US | 501 (C) | Randomized, placebo-controlled, double-blind, adaptive trial | Sepsis with acute respiratory or cardiovascular organ dysfunction | Vasopressor and ventilator-free days at 30 days after randomization | NCT03509350 |
Metabolic Resuscitation Using Ascorbic Acid, Thiamine, and Glucocorticoids in Sepsis (ORANGES) | Two centers | NJ, US | 140 (C) | Randomized, double-blind placebo-controlled trial | Sepsis/septic shock | Time to vasopressor independence (hours) through study completion; Change in SOFA score at 4 days post-randomization | NCT03422159 |
The Vitamin C, Hydrocortisone and Thiamine in Patients with Septic Shock Trial (VITAMINS) | Multicenter | Australia, New Zealand, Brazil | 216 (C) | Randomized, placebo-controlled trial | Sepsis/septic shock | Time alive and free of vasopressors at day 7 (168 hours) after randomization. | NCT03333278 |
Thiamine, Vitamin C and Hydrocortisone in the Treatment of Septic Shock | Single center | Michigan, US | 60 (T) (R) | Placebo-controlled trial | Septic shock | Mortality rate compared to Marik’s 2017 study5 | NCT03540628 |
Hydrocortisone, Vitamin C, and Thiamine for the Treatment of Sepsis and Septic Shock (HYVCTTSSS) | Single center | Guangdong, China | 80 (C) | Randomized, placebo-controlled trial | Sepsis/septic shock | Hospital survival at 14 days | NCT03258684 |
Pilot Study on the Use of Hydrocortisone, Vitamin C and Thiamine in Patient with Sepsis and Septic Shock | Single center | Girona, Spain | 40(T) (R) | Placebo-controlled trial | Septic shock and multiorgan failure | 28-day mortality | NCT04111822 |
Outcomes of Septic Shock Patients Treated with a Metabolic Resuscitation Bundle Consisting of Intravenous Hydrocortisone, Ascorbic Acid and Thiamine) | Single center | Wisconsin, US | 80 (T) (NR) | Placebo-controlled trial | Sepsis/septic shock | Duration of vasopressors at study conclusion, up to 3 months | NCT03913468 |
Vitamin C, Thiamine and Hydrocortisone for the Treatment of Septic Shock | Single center | Yangzhou, China | 406 (T) (R) | Placebo-controlled trial | Sepsis/septic shock | 90-day mortality | NCT03872011 |
Effect of IV Vitamin C, Thiamine, and Steroids on Mortality of Septic Shock | Single center | NY, US | 130(T) (R) | Placebo-controlled trial | Sepsis/septic shock | 30-day mortality | NCT03828929 |
Evaluation of Hydrocortisone, Vitamin C and Thiamine for the Treatment of Septic Shock (HYVITS) | Single center | Doha, Qatar | 216 (T) (R) | Prospective, randomized, two-arm parallel-group trial | Sepsis/septic shock | 60-day mortality | NCT03380507 |
Vitamin C, Hydrocortisone and Thiamine for Septic Shock (CORVICTES) | Single center | Athens, Greece | 400 (T) (R) | Placebo-controlled trial | Septic shock | Cerebral autoregulation 24–78 hours after randomization; Cerebral blood flow 24–78 hours after randomization | NCT03592693 |
Vitamin C, Steroids, and Thiamine, and Cerebral Autoregulation and Functional Outcome in Septic Shock (CORVICTES-ϒM) | Single center | Athens, Greece | 100 (T) (R) | Placebo-controlled trial | Septic shock | Cerebral autoregulation 24–78 hours after randomization; Cerebral blood flow 24–78 hours after randomization | NCT03649633 |
Therapy With Hydrocortisone, Ascorbic Acid, Thiamine in Patients With Sepsis | Single center | Tanta, Egypt | 80 (T) (NR) | Placebo-controlled trial | Sepsis/septic shock | Change in SOFA score at 28 days and procalcitonin level | NCT04160676 |
C-Completed, T-Target, R-Recruiting, NR-Not Recruiting