Could vitamin c save lives after cardiac arrest? new trial investigates
NCT ID NCT05817851
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This phase 2 trial tests whether giving high-dose vitamin C and thiamine early after cardiac arrest can help patients recover from shock. About 234 adults who remain unconscious after cardiac arrest and need blood pressure support will be randomly assigned to get either standard care or standard care plus high-dose vitamin C for three days. The main goal is to see if vitamin C helps patients come off blood pressure medication faster.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- high-dose vitamin C (ascorbic acid) plus thiamine (vitamin B1)
- What this could lead to
- If it works, this could offer a simple, safe way to reduce shock and organ failure after cardiac arrest, potentially improving survival and brain recovery.
- What could go wrong
- This is an early phase 2 trial with 234 participants, so results are not definitive. High-dose vitamin C may not improve outcomes and could cause side effects like kidney stones.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 234 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Dec 2023
- Expected to finish
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Jan 2028
An estimate. End dates often move.
- Lead sponsor
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A research network
The lead sponsor is a research network or cooperative group.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * patients still comatose (Glasgow coma scale \< 8) after an OHCA of presumed cardiac origin with ROSC \< 60 min; * and treated with a norepinephrin or an epinephrin continuous infusion during at least 30 min before randomization to maintain mean arterial pressure (MAP) ≥ 65 mmHg. Exclusion Criteria: * patients still comatose (Glasgow coma scale \< 8) after an OHCA of presumed cardiac origin with ROSC \< 60 min; * and treated with a norepinephrin or an epinephrin continuous infusion ≥ 0.2µg/kg/h, within 4 hours after OHCA, during at least 30 min/h to maintain mean arterial pressure (MAP) ≥ 65 mmHg. Exclusion criteria: * minor or pregnant women; * OHCA from evident extracardiac cause (trauma, bleeding, poisoning, etc.); * interval between RACS and randomization \> 6 hours; * extracorporeal circulatory assistance requirement in the first 4 hours after OHCA; * history of urolithiasis, oxalate nephropathy or hemochromatosis; * glucose-6-phosphate deshydrogenase deficiency; nephrolithiasis, hyperoxalyurie * patients already treated with vit-C; known vit-C deficit; * inclusion in another study; * pre-existent severe chronic kidney disease (glomerular filtration rate \< 30ml/min); * treatment limitationsor moribound * Patient with derpived freedom or with legal protective measures. * Patient not covered by French national health insurance
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
10 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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CH d'Arras
RECRUITINGArras, France
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CH de Melun (GHSIF)
ACTIVE_NOT_RECRUITINGMelun, France
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CH de Versailles
NOT_YET_RECRUITINGVersailles, France
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CHI Nord-Ardennes
ACTIVE_NOT_RECRUITINGCharleville-Mézières, France
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Centre Hospitalier Béthune
RECRUITINGBéthune, 62408, France
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Centre Hospitalier Toulon La Seyne sur Mer
RECRUITINGToulon, France
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Centre Hospitalier Universitaire d'Amiens
ACTIVE_NOT_RECRUITINGAmiens, France
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Centre Hospitalier Universitaire de LILLE
RECRUITINGLille, France
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Centre Hospitalier de Dieppe
RECRUITINGDieppe, France
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Centre Hospitalier de LENS
RECRUITINGLens, 62307, France
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Centre Hospitalier de Rouen
RECRUITINGRouen, France
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Centre Hospitalier de Valenciennes
ACTIVE_NOT_RECRUITINGValenciennes, France
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GHEF Site Marne La Vallée
RECRUITINGJossigny, France
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Hôpital Lariboisière
RECRUITINGParis, 75475, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can Fine-Tuning brain pressure save hearts and minds?
- Ultrasound may outperform human hands in detecting pulse during cardiac arrest
- How high should blood pressure go after cardiac arrest? trial tests two targets
- Can tracking ambulance ventilators improve emergency breathing care?
- Blood tests may reveal brain recovery after cardiac arrest
- Can cooling after cardiac arrest change how the body burns fuel?