Condition: Cardiac Arrest · Neurologic Symptoms · Intensive Care Neurological Disorder · Sponsor: Nantes University Hospital
Cerebral lesions are responsible for two thirds of deaths in patients admitted to intensive care following cardiac arrest. Patients with neurological lesions should be the priority target for neuroprotective interventions, which are the cornerstone of post-cardiac arrest care (allowing a reduction in the burden of care for patients without this type of lesion). Furthermore, these interventions must be based on a precise assessment of the severity of these brain lesions: carrying out neuro-protective interventions in patients without brain lesions exposes these patients to unnecessary treatment potentially associated with adverse effects without any possible benefit. However, the early assessment of neurological prognosis, particularly on admission to intensive care, is an area where there is little research and where it is not possible to obtain a precise and reproducible assessment. Several tools can be used to assess this prognosis at an early stage: anamnesis and characteristics of the cardiac arrest and the patient's comorbidities, imaging, electrophysiology and biomarkers. To assess the predictive value of early biomarker testing in patients resuscitated after cardiac arrest, whatever the cause, the investigators plan to conduct a prospective observational multicentre trial. It is important to bear in mind that the aim of this study is not to assess the long-term prognosis of patients suffering cardiac arrest in order to take measures to limit or discontinue active the…
This description comes directly from the study's public registry record.
Jean-Baptiste LASCARROU · 0240087386 · jeanbaptiste.lascarrou@chu-nantes.fr
Always discuss trial participation with your own doctor first.
| CHD Vendée | La Roche-sur-Yon, France | Recruiting |
| CHU Nantes | Nantes, France | Recruiting |
| APHP - Hôpital Cochin | Paris, France | Recruiting |
| CH Saint-Nazaire | Saint-Nazaire, France | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06387225