Dexmedetomidine Trial for Effects on Rhythms, Sleep Architecture, and Biomarker Dynamics in Older Adults (DEXTER)
Dexmedetomidine Trial for Effects on Rhythms, Sleep Architecture, and Biomarker Dynamics - A Pilot Study (DEXTER)
調査の概要
詳細な説明
Circadian rhythms are fundamental regulators of human physiology, coordinating sleep-wake timing, neural activity, metabolic processes, and hormonal signaling across the 24-hour day. These endogenous rhythms are coordinated by the suprachiasmatic nucleus (SCN), the central circadian pacemaker in the hypothalamus that integrates environmental cues such as light to synchronize peripheral and central biological processes. In older adults, circadian rhythms often degrade, exhibiting reduced robustness and impaired alignment with behavioral cycles. Such alterations are closely linked to disrupted sleep architecture, particularly sleep fragmentation and loss of restorative non-rapid eye movement (NREM) sleep. Crucially, sleep and circadian dysfunction is increasingly recognized as a critical modulator of neurodegenerative biomarker dynamics. Experimental evidence suggests that fragmented sleep and reduced slow-wave sleep directly alter the production, release, and clearance of neurotoxic proteins, leading to elevated tau levels. These observations highlight a potential mechanistic pathway linking sleep-circadian dysfunction to neurodegeneration and underscore the need to understand how interventions that stabilize these systems influence the temporal profile of tau-related biomarkers. Dexmedetomidine, a highly selective alpha2-adrenergic receptor agonist, represents a unique pharmacologic probe for investigating the links between sleep architecture, circadian physiology, and tau biomarker dynamics. Unlike traditional sedatives, dexmedetomidine engages endogenous sleep-promoting pathways and produces a NREM-like state characterized by electrophysiologic features resembling natural sleep. Beyond its sleep-modulating properties, emerging preclinical evidence suggests that dexmedetomidine exerts potent chronobiotic effects (i.e., the ability to stabilize or entrain circadian rhythms). For instance, preclinical models indicate it activates vasoactive intestinal peptide (VIP) neurons within the SCN and modulates circadian entrainment processes. Clinical studies of thoracic surgery patients further suggest that dexmedetomidine may preserve endogenous circadian signaling, such as melatonin secretion, during the early postoperative period. The recent development of sublingual dexmedetomidine (SL Dex) provides a transformative, noninvasive formulation that enables controlled administration outside of intensive care settings, distinguishing it from traditional intravenous (IV) dexmedetomidine, which is typically limited to monitored environments. Preliminary studies have suggested that SL Dex produces measurable changes in sleep architecture, including increased slow-wave activity, shortened sleep latency, and prolonged REM sleep latency. However, the extent to which SL Dex influences circadian regulation, sleep architecture, and the temporal profile of tau biomarkers across the 24-hour sleep-wake cycle in humans has not been systematically characterized. Addressing this gap requires a rigorously controlled experimental approach capable of isolating the physiologic effects of SL Dex from environmental and behavioral confounders. Prior clinical studies have largely occurred in perioperative or other medically complex settings in which surgery, pain, inflammation, environmental disruption, concomitant medications, and irregular behaviors may confound interpretation of sleep and circadian outcomes. An in-laboratory protocol that standardizes light exposure, posture, feeding, activity, and sampling timing provides a necessary platform to isolate these effects. Determining whether SL Dex produces not only sleep-like sedation, but also measurable sleep/circadian effects and tau dynamics would provide important insights into the relationship between pharmacologic modulation of sleep-circadian biology and inform future translational studies in aging and neurobiology.
Specific Aims and Objectives: This study aims to evaluate the feasibility, safety, and physiologic effects of sublingual dexmedetomidine (SL Dex) on sleep architecture, circadian physiology, and tau biomarker dynamics in older adults under controlled laboratory conditions. SL Dex represents a novel, noninvasive approach to modulating sleep and circadian biology and provides a unique opportunity to examine downstream effects on neurodegenerative biomarkers. Specifically, this study aims to:
- Assess the feasibility and safety of administering SL Dex within a controlled in-laboratory sleep and circadian protocol with ambulatory follow-up.
- Quantify the acute effects of SL Dex on sleep architecture, circadian physiology, and tau dynamics under controlled experimental conditions.
- Characterize the duration and trajectory of SL Dex-associated effects on sleep and circadian physiology during ambulatory follow-up.
研究の種類
入学 (推定)
段階
- 初期フェーズ 1
連絡先と場所
研究連絡先
- 名前:Chenlu Gao, PhD
- 電話番号:617-643-9515
- メール:cgao6@mgh.harvard.edu
研究場所
-
-
Massachusetts
-
Boston、Massachusetts、アメリカ、02115
- Brigham and Women's Hospital
-
コンタクト:
- Peng Li, PhD
- 電話番号:617-643-9514
- メール:pli9@mgh.harvard.edu
-
Boston、Massachusetts、アメリカ、02129
- Massachusetts General Hospital
-
-
参加基準
適格基準
就学可能な年齢
- 高齢者
健康ボランティアの受け入れ
説明
Inclusion Criteria:
- Age 65 years or older
- Able to provide informed consent
- Willing and able to comply with all study procedures, including in-laboratory and ambulatory monitoring
- Able to provide informed consent using an IRB-approved translated consent document (when available) and complete study procedures with translated materials and/or qualified interpreter services, if needed- Stable residence and sleep schedule sufficient to complete study monitoring periods
- Able to safely discontinue or adjust medications that may interfere with study procedures or outcomes, as determined by the study investigator
Exclusion Criteria:
- Clinically significant sleep disorders including narcolepsy, severe obstructive sleep apnea, REM sleep behavior disorder, or periodic limb movement disorder
- Clinically significant cardiovascular disease including bradyarrhythmia, conduction abnormalities, heart failure, cardiomyopathy, ischemic heart disease, or conditions increasing risk with dexmedetomidine
- Known QT prolongation, clinically significant arrhythmias, symptomatic bradycardia, hypokalemia, hypomagnesemia, or concurrent use of QT-prolonging medications
- Contraindication or allergy to dexmedetomidine or study medications
- Severe hepatic impairment
- Neurologic, psychiatric, or substance use disorders that may interfere with participation or data interpretation
- Use of medications significantly affecting sleep, circadian rhythms, or cardiovascular function
- Gastrointestinal conditions increasing risk of capsule retention or bowel obstruction
- Swallowing disorders or aspiration risk
- Presence of implantable electronic medical devices
- Use of anticoagulant or antiplatelet medications increasing bleeding risk
- Pregnancy or breastfeeding
- Shift work or frequent travel across more than two time zones
- Participation in another interventional study that may interfere with study participation or interpretation of results
- Anticipated need for MRI during the period in which the ingestible telemetry capsule may remain in the body
- Inability to tolerate study procedures (blood draws, PSG, wearable devices, ingestible capsule)
- Unable to provide informed consent even with translated materials/interpreter support
- Previous participation in this trial
- Concurrent interventional studies that may interfere with participation
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:支持療法
- 割り当て:ランダム化
- 介入モデル:クロスオーバー割り当て
- マスキング:トリプル
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的:Sublingual Dexmedetomidine First
Participants receive a single 120 mcg dose of sublingual dexmedetomidine (IGALMI®) during the first in-laboratory study period and matched placebo during the second study period after a washout interval of at least 3 weeks.
The study evaluates effects on sleep architecture, circadian physiology, and plasma tau biomarker dynamics under controlled laboratory conditions.
|
Participants receive a single 120 mcg dose of sublingual dexmedetomidine (IGALMI®) administered approximately 15-20 minutes before the scheduled sleep opportunity during the in-laboratory protocol.
Participants receive a matched placebo sublingual film identical in appearance, packaging, and administration method to the active dexmedetomidine formulation but containing no active medication.
|
|
プラセボコンパレーター:Placebo First
Participants receive matched placebo during the first in-laboratory study period and a single 120 mcg dose of sublingual dexmedetomidine (IGALMI®) during the second study period after a washout interval of at least 3 weeks.
The study evaluates effects on sleep architecture, circadian physiology, and plasma tau biomarker dynamics under controlled laboratory conditions.
|
Participants receive a single 120 mcg dose of sublingual dexmedetomidine (IGALMI®) administered approximately 15-20 minutes before the scheduled sleep opportunity during the in-laboratory protocol.
Participants receive a matched placebo sublingual film identical in appearance, packaging, and administration method to the active dexmedetomidine formulation but containing no active medication.
|
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Number of Participants With Adverse Events
時間枠:From first study intervention through completion of the 10-day ambulatory follow-up following the second study period
|
Number of participants experiencing one or more adverse events during the study, including hypotension, bradycardia, and excessive sedation.
|
From first study intervention through completion of the 10-day ambulatory follow-up following the second study period
|
|
Proportion of Participants Completing the Study
時間枠:Through completion of the 10-day ambulatory follow-up following the second study period
|
Proportion of enrolled participants who complete both study periods, including the in-laboratory protocols and post-laboratory ambulatory follow-up.
|
Through completion of the 10-day ambulatory follow-up following the second study period
|
|
Proportion of Consented Participants Who Are Randomized
時間枠:At randomization, prior to the first study intervention
|
Proportion of participants who provide informed consent and are subsequently randomized to a study intervention sequence, calculated as the number of randomized participants divided by the total number of participants who provide informed consent.
|
At randomization, prior to the first study intervention
|
|
Proportion of Participants Completing the In-Laboratory Protocol
時間枠:Through completion of the second 3-night in-laboratory study period
|
Proportion of enrolled participants who complete the 3-night in-laboratory protocol during both study periods.
|
Through completion of the second 3-night in-laboratory study period
|
|
Proportion of Participants Completing Ambulatory Follow-Up
時間枠:Through completion of the 10-day ambulatory follow-up following the second study period
|
Proportion of enrolled participants who complete the 10-day post-laboratory ambulatory monitoring period during both study periods.
|
Through completion of the 10-day ambulatory follow-up following the second study period
|
|
Proportion of Required Actigraphy Monitoring Completed
時間枠:Through completion of the 10-day ambulatory follow-up following the second study period
|
Proportion of required actigraphy monitoring completed by participants across the pre-laboratory and post-laboratory ambulatory monitoring periods.
|
Through completion of the 10-day ambulatory follow-up following the second study period
|
|
Proportion of Required Polysomnography Assessments Completed
時間枠:Through completion of the second 3-night in-laboratory study period
|
Proportion of required in-laboratory polysomnography assessments completed by participants.
|
Through completion of the second 3-night in-laboratory study period
|
|
Proportion of Required Wearable EEG Assessments Completed
時間枠:Through completion of the 10-day ambulatory follow-up following the second study period
|
Proportion of required ambulatory wearable EEG assessments completed by participants.
|
Through completion of the 10-day ambulatory follow-up following the second study period
|
|
Proportion of Required Sleep Diaries Completed
時間枠:Through completion of the 10-day ambulatory follow-up following the second study period
|
Proportion of required sleep diary assessments completed by participants during ambulatory monitoring.
|
Through completion of the 10-day ambulatory follow-up following the second study period
|
|
Number of Participants Withdrawing Due to Adverse Effects
時間枠:From first study intervention through completion of the 10-day ambulatory follow-up following the second study period
|
Number of participants who withdraw from the study or discontinue study procedures because of adverse effects.
|
From first study intervention through completion of the 10-day ambulatory follow-up following the second study period
|
|
Heart Rate Before and After Study Drug Administration
時間枠:Pre-dose and post-dose on Day 2 of each 3-day in-laboratory study period
|
Heart rate measured before and after administration of sublingual dexmedetomidine or placebo to assess hemodynamic safety and tolerability.
Heart rate will be reported in beats per minute.
|
Pre-dose and post-dose on Day 2 of each 3-day in-laboratory study period
|
|
Systolic Blood Pressure Before and After Study Drug Administration
時間枠:Pre-dose and post-dose on Day 2 of each 3-day in-laboratory study period
|
Systolic blood pressure measured before and after administration of sublingual dexmedetomidine or placebo to assess hemodynamic safety and tolerability.
Systolic blood pressure will be reported in mm Hg.
|
Pre-dose and post-dose on Day 2 of each 3-day in-laboratory study period
|
|
Diastolic Blood Pressure Before and After Study Drug Administration
時間枠:Pre-dose and post-dose on Day 2 of each 3-day in-laboratory study period
|
Diastolic blood pressure measured before and after administration of sublingual dexmedetomidine or placebo to assess hemodynamic safety and tolerability.
Diastolic blood pressure will be reported in mm Hg.
|
Pre-dose and post-dose on Day 2 of each 3-day in-laboratory study period
|
|
Proportion of Required Blood Samples Collected
時間枠:Through completion of the second 3-night in-laboratory study period
|
Proportion of protocol-specified blood samples successfully collected during the in-laboratory study periods.
|
Through completion of the second 3-night in-laboratory study period
|
|
Number of Participants Unable to Complete a Study Procedure Due to Intolerance
時間枠:From enrollment through completion of the 10-day ambulatory follow-up following the second study period
|
Number of participants who are unable to complete one or more protocol-specified study procedures because of intolerance, including blood draws or physiologic monitoring procedures.
|
From enrollment through completion of the 10-day ambulatory follow-up following the second study period
|
|
Proportion of Required Core Body Temperature Capsule Assessments Completed
時間枠:Pre-laboratory Day 6, continuously during the 3-day in-laboratory protocol, and post-laboratory Days 4 and 6 during each study period
|
Proportion of required core body temperature assessments using the ingestible telemetry capsule that are completed by participants across the pre-laboratory, in-laboratory, and post-laboratory monitoring periods.
|
Pre-laboratory Day 6, continuously during the 3-day in-laboratory protocol, and post-laboratory Days 4 and 6 during each study period
|
|
Proportion of Participants Adherent to Required Caffeine Restrictions
時間枠:From 72 hours before admission through completion of the 3-night in-laboratory protocol during each study period
|
Proportion of participants who adhere to protocol-specified caffeine restrictions during required study monitoring periods.
|
From 72 hours before admission through completion of the 3-night in-laboratory protocol during each study period
|
|
Proportion of Participants Adherent to Required Alcohol Restrictions
時間枠:From 24 hours before admission through completion of the 3-night in-laboratory protocol during each study period
|
Proportion of participants who adhere to protocol-specified alcohol restrictions during required study monitoring periods.
|
From 24 hours before admission through completion of the 3-night in-laboratory protocol during each study period
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Dim Light Melatonin Onset (DLMO) timing
時間枠:During the 3-hour dim-light period preceding habitual bedtime on each in-laboratory study day
|
Circadian phase assessed using dim light melatonin onset derived from serial plasma melatonin sampling during controlled dim-light conditions.
|
During the 3-hour dim-light period preceding habitual bedtime on each in-laboratory study day
|
|
Sleep Latency Measured by Polysomnography
時間枠:Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
Sleep latency, defined as the time from lights out to sleep onset, measured by overnight polysomnography.
|
Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
|
Total Sleep Time Measured by Polysomnography
時間枠:Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
Total time spent asleep during the overnight sleep period, measured by polysomnography and reported in minutes.
|
Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
|
Sleep Efficiency Measured by Polysomnography
時間枠:Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
Sleep efficiency measured by polysomnography, calculated as total sleep time divided by time in bed multiplied by 100 and reported as a percentage.
|
Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
|
Wake After Sleep Onset Measured by Polysomnography
時間枠:Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
Total time spent awake after initial sleep onset and before final awakening, measured by polysomnography and reported in minutes.
|
Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
|
REM Sleep Latency Measured by Polysomnography
時間枠:Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
Time from sleep onset to the first epoch of rapid eye movement (REM) sleep, measured by polysomnography and reported in minutes.
|
Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
|
Percentage of Total Sleep Time Spent in N2 Sleep Measured by Polysomnography
時間枠:Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
Percentage of total sleep time classified as stage N2 sleep based on polysomnography.
|
Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
|
Percentage of Total Sleep Time Spent in N3 Sleep Measured by Polysomnography
時間枠:Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
Percentage of total sleep time classified as stage N3 sleep based on polysomnography.
|
Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
|
Percentage of Total Sleep Time Spent in REM Sleep Measured by Polysomnography
時間枠:Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
Percentage of total sleep time classified as rapid eye movement (REM) sleep based on polysomnography.
|
Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
|
Phase of the Core Body Temperature Circadian Rhythm
時間枠:Continuously across the 3-day in-laboratory protocol during each study period
|
Circadian phase of the core body temperature rhythm derived from continuous core body temperature monitoring using a rectal thermistor
|
Continuously across the 3-day in-laboratory protocol during each study period
|
|
Amplitude of the Core Body Temperature Circadian Rhythm
時間枠:Continuously across the 3-day in-laboratory protocol during each study period
|
Amplitude of the core body temperature rhythm derived from continuous core body temperature monitoring using a rectal thermistor.
|
Continuously across the 3-day in-laboratory protocol during each study period
|
|
Amplitude of the Melatonin Rhythm
時間枠:Across the 3-day in-laboratory protocol during each study period
|
Amplitude of the melatonin rhythm derived from serial plasma melatonin concentrations collected under controlled in-laboratory conditions.
|
Across the 3-day in-laboratory protocol during each study period
|
|
EEG Delta Oscillation Power
時間枠:Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
Delta-band EEG power derived from quantitative EEG spectral analysis during overnight polysomnography and reported in squared microvolts (µV²).
|
Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
|
EEG Delta Oscillation Power Density
時間枠:Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
Delta-band EEG power spectral density derived from quantitative EEG spectral analysis during overnight polysomnography and reported in squared microvolts per hertz (µV²/Hz).
|
Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
|
EEG Slow Oscillation Power
時間枠:Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
Slow-oscillation EEG power derived from quantitative EEG spectral analysis during overnight polysomnography and reported in squared microvolts (µV²).
|
Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
|
EEG Theta Oscillation Power
時間枠:Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
Theta-band EEG power derived from quantitative EEG spectral analysis during overnight polysomnography and reported in squared microvolts (µV²).
|
Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
|
EEG Alpha Oscillation Power
時間枠:Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
Alpha-band EEG power derived from quantitative EEG spectral analysis during overnight polysomnography and reported in squared microvolts (µV²).
|
Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
|
EEG Beta Oscillation Power
時間枠:Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
Beta-band EEG power derived from quantitative EEG spectral analysis during overnight polysomnography and reported in squared microvolts (µV²).
|
Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
|
EEG Sigma Oscillation Power During NREM Sleep
時間枠:Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
Sigma-band EEG power derived from quantitative EEG spectral analysis during non-rapid eye movement (NREM) sleep stages and reported in squared microvolts (µV²).
|
Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
|
EEG Slow-Wave Amplitude
時間枠:Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
Mean amplitude of detected EEG slow waves derived from quantitative EEG analysis during overnight polysomnography and reported in microvolts (µV).
|
Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
|
EEG Slow-Wave Slope
時間枠:Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
Mean slope of detected EEG slow waves derived from quantitative EEG analysis during overnight polysomnography and reported in microvolts per second (µV/s).
|
Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
|
Sleep Spindle Density During NREM Sleep
時間枠:Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
Density of detected sleep spindles derived from quantitative EEG analysis during non-rapid eye movement (NREM) sleep stages and reported as the number of spindles per minute.
|
Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
|
Sleep Spindle Frequency During NREM Sleep
時間枠:Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
Mean frequency of detected sleep spindles derived from quantitative EEG analysis during non-rapid eye movement (NREM) sleep stages and reported in hertz (Hz).
|
Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
|
Sleep Spindle Duration During NREM Sleep
時間枠:Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
Mean duration of detected sleep spindles derived from quantitative EEG analysis during non-rapid eye movement (NREM) sleep stages and reported in seconds.
|
Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
|
Sleep Spindle Amplitude During NREM Sleep
時間枠:Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
Mean amplitude of detected sleep spindles derived from quantitative EEG analysis during non-rapid eye movement (NREM) sleep stages and reported in microvolts (µV).
|
Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
|
Time Spent in N1 Sleep Measured by Polysomnography
時間枠:Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
Total time classified as stage N1 sleep based on polysomnography and reported in minutes.
|
Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
|
Time Spent in N2 Sleep Measured by Polysomnography
時間枠:Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
Total time classified as stage N2 sleep based on polysomnography and reported in minutes.
|
Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
|
Time Spent in N3 Sleep Measured by Polysomnography
時間枠:Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
Total time classified as stage N3 (slow-wave) sleep based on polysomnography and reported in minutes.
|
Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
|
Time Spent in REM Sleep Measured by Polysomnography
時間枠:Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
Total time classified as rapid eye movement (REM) sleep based on polysomnography and reported in minutes.
|
Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
|
EEG Slow-Wave Density
時間枠:Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
Density of detected EEG slow waves derived from quantitative EEG analysis during overnight polysomnography and reported as the number of slow waves per minute.
|
Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
|
Percentage of Total Sleep Time Spent in N1 Sleep Measured by Polysomnography
時間枠:Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
Percentage of total sleep time classified as stage N1 sleep based on polysomnography.
|
Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
|
その他の成果指標
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Plasma p-tau217 Concentrations Across the 24-Hour Sleep-Wake Cycle
時間枠:Across the 24-hour sleep-wake cycle during each in-laboratory study period
|
Serial plasma phosphorylated tau 217 (p-tau217) concentrations measured from venous blood samples collected every 4 hours across the 24-hour sleep-wake cycle, with additional hourly sampling during the 3-hour dim-light period preceding habitual bedtime, to characterize temporal p-tau217 dynamics under sublingual dexmedetomidine and placebo conditions.
|
Across the 24-hour sleep-wake cycle during each in-laboratory study period
|
|
Sleep Onset Time Measured by Wrist Actigraphy
時間枠:Days 1-7 of the pre-laboratory monitoring period and Days 1-10 of the post-laboratory ambulatory monitoring period during each study period
|
Sleep onset time derived from wrist-worn actigraphy during ambulatory monitoring.
|
Days 1-7 of the pre-laboratory monitoring period and Days 1-10 of the post-laboratory ambulatory monitoring period during each study period
|
|
Total Sleep Time Measured by Wrist Actigraphy
時間枠:Days 1-7 of the pre-laboratory monitoring period and Days 1-10 of the post-laboratory ambulatory monitoring period during each study period
|
Total sleep time derived from wrist-worn actigraphy during ambulatory monitoring and reported in minutes.
|
Days 1-7 of the pre-laboratory monitoring period and Days 1-10 of the post-laboratory ambulatory monitoring period during each study period
|
|
Sleep Fragmentation Index Measured by Wrist Actigraphy
時間枠:Days 1-7 of the pre-laboratory monitoring period and Days 1-10 of the post-laboratory ambulatory monitoring period during each study period
|
Sleep fragmentation index derived from wrist-worn actigraphy during ambulatory monitoring.
|
Days 1-7 of the pre-laboratory monitoring period and Days 1-10 of the post-laboratory ambulatory monitoring period during each study period
|
|
Sleep Efficiency Measured by Wrist Actigraphy
時間枠:Days 1-7 of the pre-laboratory monitoring period and Days 1-10 of the post-laboratory ambulatory monitoring period during each study period
|
Sleep efficiency derived from wrist-worn actigraphy during ambulatory monitoring and reported as a percentage.
|
Days 1-7 of the pre-laboratory monitoring period and Days 1-10 of the post-laboratory ambulatory monitoring period during each study period
|
|
Core Body Temperature Circadian Rhythm Phase During Ambulatory Monitoring
時間枠:Day 6 of the 7-day pre-laboratory monitoring period and Days 4 and 6 of the 10-day post-laboratory ambulatory monitoring period during each study period
|
Circadian phase of the core body temperature rhythm derived from continuous core body temperature monitoring using an ingestible telemetry capsule during pre-laboratory and post-laboratory ambulatory monitoring.
|
Day 6 of the 7-day pre-laboratory monitoring period and Days 4 and 6 of the 10-day post-laboratory ambulatory monitoring period during each study period
|
|
Core Body Temperature Circadian Rhythm Amplitude During Ambulatory Monitoring
時間枠:Day 6 of the 7-day pre-laboratory monitoring period and Days 4 and 6 of the 10-day post-laboratory ambulatory monitoring period during each study period
|
Amplitude of the core body temperature circadian rhythm derived from continuous core body temperature monitoring using an ingestible telemetry capsule during pre-laboratory and post-laboratory ambulatory monitoring.
|
Day 6 of the 7-day pre-laboratory monitoring period and Days 4 and 6 of the 10-day post-laboratory ambulatory monitoring period during each study period
|
|
Subjective Sleep Quality Rating From Daily Sleep Diary
時間枠:Daily during Days 1-7 of the pre-laboratory monitoring period and Days 1-10 of the post-laboratory ambulatory monitoring period during each study period
|
Subjective sleep quality assessed using a daily sleep diary on an 11-point numeric rating scale ranging from 0 (very poor) to 10 (excellent), with higher scores indicating better subjective sleep quality.
|
Daily during Days 1-7 of the pre-laboratory monitoring period and Days 1-10 of the post-laboratory ambulatory monitoring period during each study period
|
|
Total Sleep Time Measured by Wearable EEG
時間枠:Nights 2 and 3 of the 7-day pre-laboratory monitoring period and Nights 1, 2, and 3 of the 10-day post-laboratory ambulatory monitoring period during each study period
|
Total sleep time derived from ambulatory wearable EEG monitoring and reported in minutes.
|
Nights 2 and 3 of the 7-day pre-laboratory monitoring period and Nights 1, 2, and 3 of the 10-day post-laboratory ambulatory monitoring period during each study period
|
|
Percentage of Total Sleep Time Spent in N3 Sleep Measured by Wearable EEG
時間枠:Nights 2 and 3 of the 7-day pre-laboratory monitoring period and Nights 1, 2, and 3 of the 10-day post-laboratory ambulatory monitoring period during each study period
|
Percentage of total sleep time classified as stage N3 sleep based on ambulatory wearable EEG monitoring.
|
Nights 2 and 3 of the 7-day pre-laboratory monitoring period and Nights 1, 2, and 3 of the 10-day post-laboratory ambulatory monitoring period during each study period
|
|
Percentage of Total Sleep Time Spent in REM Sleep Measured by Wearable EEG
時間枠:Nights 2 and 3 of the 7-day pre-laboratory monitoring period and Nights 1, 2, and 3 of the 10-day post-laboratory ambulatory monitoring period during each study period
|
Percentage of total sleep time classified as rapid eye movement (REM) sleep based on ambulatory wearable EEG monitoring.
|
Nights 2 and 3 of the 7-day pre-laboratory monitoring period and Nights 1, 2, and 3 of the 10-day post-laboratory ambulatory monitoring period during each study period
|
|
Time Spent in N1 Sleep Measured by Wearable EEG
時間枠:Nights 2 and 3 of the 7-day pre-laboratory monitoring period and Nights 1, 2, and 3 of the 10-day post-laboratory ambulatory monitoring period during each study period
|
Total time classified as stage N1 sleep based on ambulatory wearable EEG monitoring and reported in minutes.
|
Nights 2 and 3 of the 7-day pre-laboratory monitoring period and Nights 1, 2, and 3 of the 10-day post-laboratory ambulatory monitoring period during each study period
|
|
Percentage of Total Sleep Time Spent in N1 Sleep Measured by Wearable EEG
時間枠:Nights 2 and 3 of the 7-day pre-laboratory monitoring period and Nights 1, 2, and 3 of the 10-day post-laboratory ambulatory monitoring period during each study period
|
Percentage of total sleep time classified as stage N1 sleep based on ambulatory wearable EEG monitoring.
|
Nights 2 and 3 of the 7-day pre-laboratory monitoring period and Nights 1, 2, and 3 of the 10-day post-laboratory ambulatory monitoring period during each study period
|
|
Time Spent in N2 Sleep Measured by Wearable EEG
時間枠:Nights 2 and 3 of the 7-day pre-laboratory monitoring period and Nights 1, 2, and 3 of the 10-day post-laboratory ambulatory monitoring period during each study period
|
Total time classified as stage N2 sleep based on ambulatory wearable EEG monitoring and reported in minutes.
|
Nights 2 and 3 of the 7-day pre-laboratory monitoring period and Nights 1, 2, and 3 of the 10-day post-laboratory ambulatory monitoring period during each study period
|
|
Percentage of Total Sleep Time Spent in N2 Sleep Measured by Wearable EEG
時間枠:Nights 2 and 3 of the 7-day pre-laboratory monitoring period and Nights 1, 2, and 3 of the 10-day post-laboratory ambulatory monitoring period during each study period
|
Percentage of total sleep time classified as stage N2 sleep based on ambulatory wearable EEG monitoring.
|
Nights 2 and 3 of the 7-day pre-laboratory monitoring period and Nights 1, 2, and 3 of the 10-day post-laboratory ambulatory monitoring period during each study period
|
|
Time Spent in N3 Sleep Measured by Wearable EEG
時間枠:Nights 2 and 3 of the 7-day pre-laboratory monitoring period and Nights 1, 2, and 3 of the 10-day post-laboratory ambulatory monitoring period during each study period
|
Total time classified as stage N3 sleep based on ambulatory wearable EEG monitoring and reported in minutes.
|
Nights 2 and 3 of the 7-day pre-laboratory monitoring period and Nights 1, 2, and 3 of the 10-day post-laboratory ambulatory monitoring period during each study period
|
|
Time Spent in REM Sleep Measured by Wearable EEG
時間枠:Nights 2 and 3 of the 7-day pre-laboratory monitoring period and Nights 1, 2, and 3 of the 10-day post-laboratory ambulatory monitoring period during each study period
|
Total time classified as rapid eye movement (REM) sleep based on ambulatory wearable EEG monitoring and reported in minutes.
|
Nights 2 and 3 of the 7-day pre-laboratory monitoring period and Nights 1, 2, and 3 of the 10-day post-laboratory ambulatory monitoring period during each study period
|
協力者と研究者
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
IPD プランの説明
IPD 共有時間枠
IPD 共有アクセス基準
IPD 共有サポート情報タイプ
- STUDY_PROTOCOL
- SAP
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
米国で製造され、米国から輸出された製品。
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。