Consciousness Prognosis Evaluation Using Olfactory Stimulations in Comatose Patients)

Recruiting N/A Interventional Study
Disorders of Consciousness Due to Severe Brain Injury
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Diagnostic
Participants needed
96 (estimated)
Sponsor
Centre Hospitalier St Anne · Other
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About This Trial
The goal of this observational study is to determine whether the clinical response to olfactory stimulation (known as the "sniff" response) can help predict 3-month neurological outcomes in ICU patients with persistent disorders of consciousness after sedation withdrawal, regardless of the reason for admission or the initial severity. The main questions this study aims to answer are: * Can the "…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Admission to neuro-intensive care unit (neuro-ICU) * Age ≥ 18 years * Patients with persistent disorders of consciousness defined by an abnormal CRS-R score (\<16) at 72 hours after sedation withdrawal and spontaneous ventilation * Consent obtained from legal representatives o…
Contacts

Eleonore BOUCHEREAU, MD, PhD

0145658902

e.bouchereau@ghu-paris.fr

CONTACT