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NLM Technical Bulletin
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A Safety and Efficacy Study of Patients Requiring Sedation for Elective Awake Fiberoptic Intubation.
This study has been completed.
Study NCT00383890 Information provided by Hospira, Inc.
First Received on October 2, 2006. Last Updated on October 8, 2007
History of Changes
Related Studies can be found by searching for the Conditions, Interventions, and Sponsors found in this study:
Conditions listed in this trial
Awake Fiberoptic Intubation
Interventions listed in this trial
More general drug interventions related to this trial
Adrenergic alpha-2 Receptor Agonists
Central Nervous System Agents
Central Nervous System Depressants
Hypnotics and Sedatives
Molecular Mechanisms of Pharmacological Action
Peripheral Nervous System Agents
Physiological Effects of Drugs
Sensory System Agents
Sponsors listed in this trial
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