Providing "Good Sleep" for ICU Sedation
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| City: |
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San Francisco |
| State: |
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California |
| Zip Code: |
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94143 |
| Conditions: |
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Sleep Disorders |
| Purpose: |
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Cognitive dysfunction, either alone or as an element in the syndrome of delirium, is a
common occurrence with an incidence as high as 75% in intensive care unit (ICU) patients and
can independently result in serious consequences including higher mortality rate. Delirium
develops through a complex interaction between the patient's baseline vulnerability (risk
factors) and precipitating factors such as disruption of sleep that may occur during
hospitalization. While sedative-hypnotic agents that are used to facilitate hypnosis and the
management of mechanically ventilated patients converge on the neural substrate that mediate
endogenous sleep, they do so at different juncture points depending on its molecular
mechanism of hypnotic action. Hypnotic agents that modulate the GABAA receptor converge at
the level of the hypothalamus while α2 adrenergic agonists converge on sleep pathways within
the brainstem. This translational project seeks to determine whether sedation mediated by
activation of α2 adrenoceptors (dexmedetomidine) is more like natural sleep than that
provided by a sedative agent that modulates the GABAA receptor (propofol). The investigators
will examine volunteers who will be monitored continuously by electroencephalography (EEG)
and whole-brain functional connectivity by magnetoencephalography (MEG) during each of three
sleep stages, namely, that induced by dexmedetomidine, propofol, or saline (natural sleep,
control). The two drug-induced sleep regimens will be compared to natural sleep using EEG
and brain connectivity by MEG
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| Study Summary: |
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In this proposal the investigators seek to determine whether sedation mediated by activation
of α2 adrenoceptors (dexmedetomidine) is more like natural sleep than that provided by a
sedative agent that modulates the GABAA receptor (propofol), two common widely used sedative
agents in ICU. Ten volunteers will be enrolled and each subject will be studied on three
experimental sessions. Subjects will be randomized to receive a continuous infusion of
either saline, dexmedetomidine (DEX), or propofol in each of the three sessions. By relying
on clinical rating scales, the investigators ensure that the doses of DEX and propofol
administered induce equisedative states before progressing to magnetoencephalography and
electroencephalography data collection.
If the restorative and reparative benefits of sleep mitigate the development of cognitive
dysfunction, this will result in shorter ICU length of stay for critically ill patients with
a concomitant reduction in healthcare costs. Furthermore, it is possible that the
restorative properties of sleep for the central nervous system can extend to the immune
system with less infection and/or greater likelihood of survival from sepsis.
In this manner, our project will translate experimental data towards clinical practice and
the adoption of rational and clinically supported interventions in the ICU that are likely
to improve not only patient reported outcome measures, but also the chance of surviving
critical illness.
Each experimental session will take a maximum of 7 hours (5 hours maximum for control
sessions).
Sessions have to be separated by at least one week. Subjects will be enrolled for a minimum
of 3 weeks (1 session on each week) and no more than 3 months.
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| Criteria: |
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Inclusion Criteria:
- Volunteer agreement and written informed consent
- Healthy female or male between 18 and 45 years of age
- Body Mass Index < 30 kg/m2
- Non-pregnant and non-lactating
- Normal airway anatomy (Mallampati class I)
Exclusion Criteria:
- Subject has a history of recent alcohol or drug abuse
- Subject is unable to communicate in English
- Subject is unwilling to meet fast guidelines (fast light meal or non-human milk for
at least 8 hours, and clear liquids at least for 2 hours prior to induction of
sedation on the day of the study)
- Subject has taken caffeine containing beverages less than 8 hours before study begins
- Subject is not able to avoid sleep for a minimum of 16 hours prior to testing
- Subject has a known allergy to either of the sedative-hypnotic drugs to be used in
the study
- Subject has abnormal airway anatomy, including loose teeth
- Subject has any family history of complications from anesthesia
- Subject has history of sleep apnea
- Subject has any reported illness, upper respiratory tract infection, abnormal vital
signs, or concerning findings on the physical exam for the past 6 weeks
- Subject has a positive urine pregnancy test
- Subject is unable to sleep supine.
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| NCT ID: |
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NCT01342328 |
| Primary Contact: |
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Principal Investigator
Mervyn Maze, MB, ChB
University of California, San Francisco
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| Backup Contact: |
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N/A |
| Location Contact: |
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San Francisco, California 94143
United States
There is no listed contact information for this specific location.
Site Status: N/A |
| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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June 19, 2013 |
| Modifications to this listing: |
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