Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-24 @ 11:44 PM
Ignite Modification Date: 2025-12-24 @ 11:44 PM
NCT ID: NCT05817851
Eligibility Criteria: 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
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Study: NCT05817851
Study Brief:
Protocol Section: NCT05817851