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WithdrawnNCT03283410

Determination of Propofol Target Concentration for Young and Elderly by Suppression Rate Analysis

Status
Withdrawn
Phase
Phase 4
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Brasilia University Hospital · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Accepted

Summary

Propofol's dose-response curve is know for the average adult but propofol's plasmatic concentration under total intravenous anesthesia differences between young and elderly must be modeled. Adaptative clinical trial (Dixon's Up and Down) for determination of ED95% of propofol concentration for hypnosis under general anesthesia for young and elderly adults.

Detailed description

Propofol's dose-response curve is know for the average adult but propofol's plasmatic concentration under total intravenous anesthesia differences between young and elderly must be modeled. Method: adaptative clinical trial (Dixon's Up and Down method) for determination of ED95% of propofol concentration (plasmatic, Marsh model) for hypnosis (BIS ranging from 40 to 60) under general anesthesia for young and elderly adults.

Conditions

Interventions

TypeNameDescription
DRUGPropofolPropofol plasmatic concentration (Marsh)

Timeline

Start date
2017-01-30
Primary completion
2017-01-30
Completion
2017-01-30
First posted
2017-09-14
Last updated
2017-09-14

Source: ClinicalTrials.gov record NCT03283410. Inclusion in this directory is not an endorsement.

Determination of Propofol Target Concentration for Young and Elderly by Suppression Rate Analysis (NCT03283410) · Clinical Trials Directory