A Study of Human Multi-Sensory Integration

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, the investigators have chosen two anesthetics with fundamentally
distinct mechanisms of action: propofol and ketamine.

The study will involve healthy compensated volunteers. On the day of the study, an EEG cap
will be applied to the participant for monitoring brain activity and an intravenous line will
be placed for drug administration. Blood pressure, ECG, pulse oxymetry, and end-tidal carbon
dioxide (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.

After this phase is complete, participants will receive either propofol or ketamine (chosen
permuted block randomization) using a clinician bolus/infusion strategy titrated to Richmond
Agitation-Sedation Scale score of -1 (see above). Once the desired sedation level is
achieved, subjects will once again complete the behavioral tasks. After the completion of
this phase (approximately 1 hour) the anesthetic dose will be increased to attain Richmond
Agitation-Sedation Scale -3 to -4. At this level of sedation subjects will not be able to do
the behavioral task and only the evoked potentials will be recorded. Upon completion of this
phase (approximately 1 hour), sedation level will be decreased to return the subject to a
Richmond Agitation-Sedation Scale of -1 and once again the tasks will be repeated.

Finally, the anesthetic infusion will be stopped. Once the Richmond Agitation-Sedation Scale
score of 0 is attained, participants will once again perform the behavioral task
(approximately 1 hour). This will conclude the experimental phase of the trial. Subjects will
be monitored until clinically established discharge criteria are met. This includes adequate
respiration, blood pressure, oxygen saturation and activity level. No formal follow-up is
required; however, subjects will be called 24 hours after study completion.

Inclusion Criteria:

- Healthy volunteers ages 18-65 years old

- American Society of Anesthesiologists (ASA) Physical Status I or II (i.e. healthy)

- Body Mass Index <30 kg/m2

- Easily visible uvula

Exclusion Criteria:

- Contraindications to administration of either propofol or ketamine

- Allergy to either one of the medications or preservative in which it is diluted.

- History (or current) seizure disorder

- Contraindications to anesthesia

- Significant cardiovascular disease (e.g. h/o hypertension, arrhythmias, myocardial
infarction, congestive heart failure, congenital heart defects, coronary artery
disease)

- Increased risk factors for difficult intubation and/or ventilation

- Obesity (BMI>=30 kg/m2)

- Mallampati class > 2.

- History of or current obstructive sleep apnea.

- Increased risk of aspiration

- Any per oral intake within 8 hours of anesthetic exposure

- Conditions that delay gastric emptying (e.g. obesity, hiatal hernia, gastro esophageal
reflux disease, pregnancy, etc.)

- Pulmonary disease (e.g. chronic obstructive pulmonary disorder, asthma requiring
rescue inhaler within last month, emphysema, pulmonary hypertension, pulmonary
fibrosis etc).

- Neurological disease. Patients with history of strokes, seizures, brain surgery,
brain tumor, increased intracranial pressure.

- Psychiatric disease. History of or presents of psychosis, schizophrenia,
schizo-affective disorder.

- Specific Medication Current Use. History of or current intake of antipsychotics
or sedatives.

- Drug abuse. History of or current use of illegal drugs such as stimulants or
depressants.

- Pregnancy or breastfeeding

- Inability to provide informed consent