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临床试验/NCT01485393
NCT01485393已完成不适用

Pilot Study Comparing the Use of Dexmedetomidine and Zolpidem to Induce Natural Sleep

Massachusetts General Hospital1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2015年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
10
试验地点
1
主要终点
Change in Sleep Quality

研究概览

简要总结

The purpose of this study is to determine whether dexmedetomidine can be used to induce normal physiological sleep in humans.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Basic Science
盲法
None

入排标准

年龄范围
18 Years 至 35 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Primary Inclusion Criteria for "Insomniac" subjects:
  • Subjects will be deemed "Insomniacs" if they suffer from any of the following:
  • Subject will be required to meet the criteria for insomnia, set by the International Classification of Sleep Disorders, which requires that a patient have difficulty initiating or maintaining sleep that is not accounted for by another sleep disorder, neurologic or psychiatric disorder or substance or medication.
  • Subject will be required to not be on any current pharmacological sleep disorder treatment.
  • Between the ages of 18 and 35 years.
  • Not taking any prescription medications that alter sleep, cognitive functions, or both.

排除标准

  • Primary Exclusion Criteria for "Healthy" control subjects:
  • Abnormal sleep habits:
  • sleeping less than 5 hours each night;
  • going to sleep before 9:00 PM or after 2:00 AM on a regular basis; or
  • Waking up before 5:00 AM or after 10:00 AM on a regular basis. This will be objectively assessed by wrist actigraphy measured for a 1-week duration prior to the first study night.
  • A sleep latency greater than 60 minutes, greater than 3 awakenings per night. This will also be objectively assessed by wrist actigraphy.
  • A score greater than or equal to 10 on the Epworth Sleepiness Scale.
  • Takes medication that alters sleep, cognitive function, or both.
  • Has a history of a known neurological or psychiatric problem.
  • Younger than 18 or older than 35 years of age.
  • Known or suspected sleep disorder(s).

研究组 & 干预措施

Healthy Control Subjects: Zolpidem, Then Dexmedetomidine

Experimental

This arm will enroll healthy control subjects, who will receive a regular nights sleep followed by a night of Zolpidem induced-sleep and then a night of Dexmedetomidine induced-sleep.

干预措施: Dexmedetomidine (Drug)

Healthy Control Subjects: Zolpidem, Then Dexmedetomidine

Experimental

This arm will enroll healthy control subjects, who will receive a regular nights sleep followed by a night of Zolpidem induced-sleep and then a night of Dexmedetomidine induced-sleep.

干预措施: Zolpidem (Drug)

Healthy Control Subjects: Dexmedetomidine, Then Zolpidem

Experimental

This arm will enroll healthy control subjects, who will receive a regular nights sleep followed by a night of Dexmedetomidine induced-sleep and then a night of Zolpidem induced-sleep.

干预措施: Dexmedetomidine (Drug)

Healthy Control Subjects: Dexmedetomidine, Then Zolpidem

Experimental

This arm will enroll healthy control subjects, who will receive a regular nights sleep followed by a night of Dexmedetomidine induced-sleep and then a night of Zolpidem induced-sleep.

干预措施: Zolpidem (Drug)

结局指标

主要结局

Change in Sleep Quality

时间窗: Approximately 8 hours

Sleep quality will be assessed objectively through EEG measures (changes from baseline in length of non-REM sleep, length of REM sleep, and length of N3 sleep--all assessed in minutes) and subjectively, utilizing a post sleep questionnaire to assess the difference in quantity of sleep (minutes) from baseline. Sleep quality is directly related to these measures of sleep quantity.

次要结局

  • Performance on a Psychomotor Vigilance Test (PVT) After Waking up From Sleep(Approximately 30 minutes after waking up)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Oluwaseun Johnson-Akeju, MD, MMSc

Assistant in Anesthaesia

Massachusetts General Hospital

研究点 (1)

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