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Propofol vs Propofol + Benzo/Opiates in High Risk Group
This study is enrolling participants by invitation only.
Study NCT01315158   Information provided by Washington University School of Medicine

First Received on March 11, 2011.   No Changes Posted
Related Studies can be found by searching for the Conditions, Interventions, and Sponsors found in this study:
Conditions listed in this trial
Sleep Apnea, Obstructive
Obesity
Additional conditions recognized in this trial
Apnea
Sleep Apnea Syndromes
More general conditions related to this trial
Body Weight
Dyssomnias
Nervous System Diseases
Nutrition Disorders
Overnutrition
Overweight
Respiration Disorders
Respiratory Tract Diseases
Signs and Symptoms
Signs and Symptoms, Respiratory
Sleep Disorders
Sleep Disorders, Intrinsic
Interventions listed in this trial
Propofol Alone
Propofol+Benzo/Opioids
Additional drug interventions recognized in this trial
Analgesics, Opioid
Fentanyl
Midazolam
Propofol
More general drug interventions related to this trial
Adjuvants, Anesthesia
Analgesics
Anesthetics
Anesthetics, General
Anesthetics, Intravenous
Anti-Anxiety Agents
Central Nervous System Agents
Central Nervous System Depressants
GABA Agents
GABA Modulators
Hypnotics and Sedatives
Molecular Mechanisms of Pharmacological Action
Narcotics
Neurotransmitter Agents
Peripheral Nervous System Agents
Pharmacologic Actions
Physiological Effects of Drugs
Psychotropic Drugs
Sensory System Agents
Therapeutic Uses
Tranquilizing Agents
Sponsors listed in this trial
Washington University School of Medicine


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