A study of human multi-sensory integration: A neurophysiologic correlate of conscious perception
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- STATUS
- Recruiting
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- participants needed
- 40
Summary
This is a prospective dual parallel arm human subject study aimed at determining the relationship between level of sedation (consciousness) and features of multi and uni-sensory evoked potentials with the ultimate goal of developing novel means of detecting consciousness under anesthesia with potential for application to other clinical settings such as brain injury. For this purpose we chose two anesthetics with fundamentally distinct mechanisms of action: propofol and ketamine. Anesthesia with ketamine currently evades adequate detection using the available monitors of depth of anesthesia. Please see the rationale for dosing of the two anesthetics above. The study will involve healthy compensated volunteers. During the screening interview we will rule out the presence of any of the exclusion criteria (see below) and explain the details of the study to the subject. After questions concerning study design are answered we will obtain consent for the participation in the study. On the day of the study, EEG cap will be applied for monitoring brain activity and IV will be placed for drug administration. Blood pressure, ECG, pulse oxymetry, and end-tidal CO2 (from nasal cannula) will be monitored. Supplemental oxygen will be administered using a nasal cannula. Subjects will then perform the behavioral tasks in the awake state for approximately 1 hour.
Details
| Condition | Anesthesia Awareness |
|---|---|
| Age | 99years or below |
| Clinical Study Identifier | 03498391 |
| Last Modified on | 19 February 2024 |
Eligibility
How to participate?
Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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