The purpose of this study is to assess the safety of ramelteon, once daily (QD), in individuals with obstructive sleep apnea.
Insomnia is characterized by difficulties initiating and maintaining sleep, or complaints of non-restorative and non-refreshing sleep. Transient insomnia affects approximately one-third to one-half of the US population, based on the results of 2 surveys of representative samples of the adult US population conducted by the Gallup Organization in which respondents were asked if they had "ever had difficulty sleeping." Based on reports of "regular" or "frequent" sleep difficulty, results from the same studies suggest that approximately one-tenth of the US population experiences chronic insomnia. The ideal treatment for insomnia would reduce the latency to onset of sleep and increase total sleep time, without a negative impact on sleep architecture and without safety concerns or next-day effects. Ramelteon is under global development by Takeda Chemical Industries, Ltd., for the treatment of transient and chronic insomnia and for the treatment of Circadian Rhythm Sleep Disorders. This study is being conducted to assess the safety of Ramelteon in subjects with obstructive sleep apnea. Participation this this study is anticipated to be about 1.5 months.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
26
Ramelteon 16 mg, tablet, orally, once daily for Periods 1 or 2 and ramelteon placebo-matching tablets, orally, once daily for Periods 1 or 2.
Unnamed facility
Birmingham, Alabama, United States
Unnamed facility
Palm Springs, California, United States
Unnamed facility
Santa Monica, California, United States
Unnamed facility
Winter Park, Florida, United States
Unnamed facility
Apnea Hypopnea Index measured by Respiratory Inductance Plethysmography (RIP)
Time frame: Periods 1 and 2.
Central Apnea Index.
Time frame: Periods 1 and 2.
Mean Oxygen Saturation for the entire night.
Time frame: Periods 1 and 2.
Obstructive Apnea Index.
Time frame: Periods 1 and 2.
Hypopnea Index.
Time frame: Periods 1 and 2.
Mean Oxygen Saturation for the entire night.
Time frame: Periods 1 and 2.
Oxygen Saturation Means for Awake Sleep Stage.
Time frame: Periods 1 and 2.
Oxygen Saturation Means for Non-Rapid Eye Movement Sleep Stage.
Time frame: Periods 1 and 2.
Oxygen Saturation Means for Rapid Eye Movement Sleep Stage.
Time frame: Periods 1 and 2.
Percentage of oxygen saturation is less than 80%.
Time frame: Periods 1 and 2.
Latency to Persistent Sleep.
Time frame: Periods 1 and 2.
Total Sleep Time.
Time frame: Periods 1 and 2.
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Cincinnati, Ohio, United States
Sleep Efficiency.
Time frame: Periods 1 and 2.
Awake Time after Persistent Sleep.
Time frame: Periods 1 and 2.
Number of Awakenings after Persistent Sleep.
Time frame: Periods 1 and 2.
Subjective Sleep Latency.
Time frame: Crossover Period 1 AM; Crossover Period 2 AM
Subjective Total Sleep Time.
Time frame: Periods 1 and 2.
Subjective Sleep Quality.
Time frame: Periods 1 and 2.
Subjective Number of Awakenings.
Time frame: Periods 1 and 2.
Subjective Ease of Falling Back to Sleep after Awakening.
Time frame: Periods 1 and 2.
Subjective Level of Alertness.
Time frame: Periods 1 and 2.
Subjective Ability to Concentrate.
Time frame: Periods 1 and 2.
Percentage of Total Sleep Time in REM sleep
Time frame: Periods 1 and 2.
Percentage of Total Sleep Time in Stage 1 NREM sleep
Time frame: Periods 1 and 2.
Percentage of Total Sleep Time in Stage 2 NREM sleep
Time frame: Periods 1 and 2.
Percentage of Total Sleep Time in Stage 3/4 NREM sleep
Time frame: Periods 1 and 2.
Percentage of Total Sleep Time in latency to REM as determined by polysomnography
Time frame: Periods 1 and 2.