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Observation and control for Neuromuscular Blockade
N/A
Recruiting
Led By 514-252-3426 Fortier, MD
Research Sponsored by Ciusss de L'Est de l'Île de Montréal
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 60 minutes
Awards & highlights
Study Summary
Gold standard for neuromuscular blockade evaluation is accelerometry in three dimensions at the thumb. There are many times that measurement at the hand can be falsely under-estimated intraoperatively secondary to constriction of the upper extremities. We believe that installing the same accelerometer at the first toe will give us similar readings for both neuromuscular blockade and recovery from rocuronium administration. This study focuses on agreement values between two accelerometers installed on the hand and at on the foot.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 60 minutes
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~60 minutes
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Time of neuromuscular blockade (NMB) recovery
Secondary outcome measures
Extubation
Neuromuscular blockade onset
Reversal
Trial Design
1Treatment groups
Experimental Treatment
Group I: Observation and controlExperimental Treatment1 Intervention
Two accelerometers will be applied on each patient; observation (foot) and control (hand, also the gold standard). Agreement values will be compared between these two monitors.
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Who is running the clinical trial?
Ciusss de L'Est de l'Île de MontréalLead Sponsor
70 Previous Clinical Trials
5,510 Total Patients Enrolled
1 Trials studying Neuromuscular Blockade
144 Patients Enrolled for Neuromuscular Blockade
514-252-3426 Fortier, MDPrincipal InvestigatorMaisonneuve-Rosemont Hospital - CIUSSS de l'Est de l'Ile de Montréal
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