Recovery of Consciousness Following Intracerebral Hemorrhage

Recruiting Observational Study
Intra Cerebral Hemorrhage
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
150 (estimated)
Sponsor
Columbia University · Other
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About This Trial
The objectives of the RECONFIG clinical study are to : 1. To identify the time to the first diagnosis of cognitive motor dissociation (CMD) in intracerebral hemorrhage (ICH) patients and to investigate whether these patients will clinically follow commands earlier after the hemorrhage. 2. To determine whether CMD independently predicts long term functional outcomes (6-month mRS scores) in ICH pat…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * 18 years or older. * Diagnosis of primary ICH (i.e., related to hypertension or anticoagulants) on Head CT and/or MRI in the frontal lobe, thalamus, or striatocapsular region. * Unresponsive to commands within 48 hours after onset of the bleed. * English, Spanish or, French as…
Contacts

Jan Claassen, MD

212-305-7236

jc1439@cumc.columbia.edu

CONTACT

Angela Velazquez, MD

212-305-6071

agv2113@cumc.columbia.edu

CONTACT