18 and older, any sex, with Cardiac Arrest or Shock. Patients with the condition only — healthy volunteers not accepted.
Results — posted to ClinicalTrials.gov
Per-arm endpoint measurements with 95% confidence intervals where reported. Source: trial results section.
LactatePrimary· 2 days
The investigators will evaluate the median lactate level over two days, compared between groups
Group
Value
95% CI
Thiamine
1.9
1.1 – 7.5
Placebo
1.8
1.2 – 5.4
Oxygen ConsumptionSecondary· 2 days
The investigators will evaluate the mean oxygen consumption over two days, compared between groups
Group
Value
95% CI
Thiamine
3.83
± 0.94
Placebo
3.48
± 1.27
Pyruvate DehydrogenaseSecondary· 2 days
The investigators will evaluate the median pyruvate dehydrogenase levels over two days, compared between groups
Group
Value
95% CI
Thiamine
1.2
0.9 – 1.5
Placebo
1.1
1.0 – 1.3
Sponsor's own description
This study is to evaluate whether thiamine can increase oxygen consumption and lower lactate in patients who initially survive an in-hospital cardiac arrest. Patients who are successfully resuscitated after an in-hospital cardiac arrest and who are on mechanical ventilation in the intensive care unit will be enrolled, and will get either thiamine or placebo. Their oxygen consumption and lactate will be measured at serial time points and compared between groups. The investigators' hypothesis is that thiamine will help restore the body's ability to metabolize oxygen normally (aerobic metabolism), leading to an increase in oxygen consumption and a decrease in lactate.
Publications & conference data
4 peer-reviewed publications reference this trial (live from Europe PMC):
NCT06322212 — Type 2 Diabetes and Blood Brain Barrier Improvement
· EARLY_PHASE1
· recruiting
NCT06298344 — The Role of Thiamine After Transcatheter Closure in Children With Left-to-Right Shunt Congenital Heart Disease
· EARLY_PHASE1
· completed
NCT03509662 — Vitamin C in Post-cardiac Arrest
· Phase 2
· completed
NCT07113769 — Plasma Biomarkers and Platelet Morphology of Extracorporeal CardioPulmonary Resuscitation
· recruiting
Other Beth Israel Deaconess Medical Center trials
Trials by the same sponsor.
NCT07352657 — Remote Alert Pathway To Optimize CaRe of Cardiac Implantable Electrical Devices: The RAPTOR-CIED Study (Main Phase)
· NA
· not yet recruiting
NCT07531602 — Effect of PEEP on Cardiac Function
· NA
· not yet recruiting
NCT07534683 — Primed to Thrive: Investigating the Combined Impact of Mindfulness Education and Meditation Practice on Psychological an
· NA
· not yet recruiting
NCT07277244 — Low-Intensity Mechanical Ventilation in the Operating Room: a Pilot Study
· NA
· enrolling by invitation
NCT06896474 — SDM POSSIBLE: A Breast Cancer Treatment Decision Aid for Women 70+ With Low-Risk Stage I Breast Cancers
· NA
· recruiting
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 Beth Israel Deaconess Medical Center
Last refreshed: 10 April 2025
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/NCT02974257.