Use of Sevoflurane to Test Concept of Cognitive Reserve
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-90
SponsorLos Angeles General Medical Center
About this trial
Previous pilot study had demonstrated a correlation between cognitive reserve and BIS variability during steady state of anesthesia. This study, we intend to evaluate the association between BIS variability and emergence and recovery time from anesthesia.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
- Minimal completion of high-school education
Adult patient < 85 years of age
No prior known history of cognitive/brain disease
ASA class I-II
Disqualifiers
- History of chronic pain
Perioperative use of anesthetic agents other than propofol, fentanyl, dilaudid, and sevoflurane
History of alcohol/substance druge abuse
Psychiatric history
Trial population
ASA I or II
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
sevoflurane
Other interventionNo intervention
Treatment groups
No treatment groups listed
Trial outcomes
Primary outcomes
1
intraoperative BIS variability
Time frame
360 minutesSecondary outcomes
1
time to recovery
Time frame
120 minutesLocations
Sponsors and contacts
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Source ClinicalTrials.gov
This trial is not recruiting at the moment. You can still explore other options: