- ICH GCP
- Registr klinických studií v USA
- Klinická studie NCT07800910
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)
Přehled studie
Postavení
Podmínky
Intervence / Léčba
Detailní popis
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.
Typ studie
Zápis (Odhadovaný)
Fáze
- Raná fáze 1
Kontakty a umístění
Studijní kontakt
- Jméno: Chenlu Gao, PhD
- Telefonní číslo: 617-643-9515
- E-mail: cgao6@mgh.harvard.edu
Studijní místa
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Massachusetts
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Boston, Massachusetts, Spojené státy, 02115
- Brigham and Women's Hospital
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Kontakt:
- Peng Li, PhD
- Telefonní číslo: 617-643-9514
- E-mail: pli9@mgh.harvard.edu
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Boston, Massachusetts, Spojené státy, 02129
- Massachusetts General Hospital
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Kritéria účasti
Kritéria způsobilosti
Věk způsobilý ke studiu
- Starší dospělý
Přijímá zdravé dobrovolníky
Popis
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
Studijní plán
Jak je studie koncipována?
Detaily designu
- Primární účel: Podpůrná péče
- Přidělení: Randomizované
- Intervenční model: Crossover Assignment
- Maskování: Trojnásobný
Zbraně a zásahy
Skupina účastníků / Arm |
Intervence / Léčba |
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Experimentální: 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.
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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.
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Komparátor placeba: 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.
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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.
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Co je měření studie?
Primární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
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Number of Participants With Adverse Events
Časové okno: From first study intervention through completion of the 10-day ambulatory follow-up following the second study period
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Number of participants experiencing one or more adverse events during the study, including hypotension, bradycardia, and excessive sedation.
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From first study intervention through completion of the 10-day ambulatory follow-up following the second study period
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Proportion of Participants Completing the Study
Časové okno: Through completion of the 10-day ambulatory follow-up following the second study period
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Proportion of enrolled participants who complete both study periods, including the in-laboratory protocols and post-laboratory ambulatory follow-up.
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Through completion of the 10-day ambulatory follow-up following the second study period
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Proportion of Consented Participants Who Are Randomized
Časové okno: At randomization, prior to the first study intervention
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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.
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At randomization, prior to the first study intervention
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Proportion of Participants Completing the In-Laboratory Protocol
Časové okno: Through completion of the second 3-night in-laboratory study period
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Proportion of enrolled participants who complete the 3-night in-laboratory protocol during both study periods.
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Through completion of the second 3-night in-laboratory study period
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Proportion of Participants Completing Ambulatory Follow-Up
Časové okno: Through completion of the 10-day ambulatory follow-up following the second study period
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Proportion of enrolled participants who complete the 10-day post-laboratory ambulatory monitoring period during both study periods.
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Through completion of the 10-day ambulatory follow-up following the second study period
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Proportion of Required Actigraphy Monitoring Completed
Časové okno: Through completion of the 10-day ambulatory follow-up following the second study period
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Proportion of required actigraphy monitoring completed by participants across the pre-laboratory and post-laboratory ambulatory monitoring periods.
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Through completion of the 10-day ambulatory follow-up following the second study period
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Proportion of Required Polysomnography Assessments Completed
Časové okno: Through completion of the second 3-night in-laboratory study period
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Proportion of required in-laboratory polysomnography assessments completed by participants.
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Through completion of the second 3-night in-laboratory study period
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Proportion of Required Wearable EEG Assessments Completed
Časové okno: Through completion of the 10-day ambulatory follow-up following the second study period
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Proportion of required ambulatory wearable EEG assessments completed by participants.
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Through completion of the 10-day ambulatory follow-up following the second study period
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Proportion of Required Sleep Diaries Completed
Časové okno: Through completion of the 10-day ambulatory follow-up following the second study period
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Proportion of required sleep diary assessments completed by participants during ambulatory monitoring.
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Through completion of the 10-day ambulatory follow-up following the second study period
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Number of Participants Withdrawing Due to Adverse Effects
Časové okno: From first study intervention through completion of the 10-day ambulatory follow-up following the second study period
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Number of participants who withdraw from the study or discontinue study procedures because of adverse effects.
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From first study intervention through completion of the 10-day ambulatory follow-up following the second study period
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Heart Rate Before and After Study Drug Administration
Časové okno: Pre-dose and post-dose on Day 2 of each 3-day in-laboratory study period
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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.
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Pre-dose and post-dose on Day 2 of each 3-day in-laboratory study period
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Systolic Blood Pressure Before and After Study Drug Administration
Časové okno: Pre-dose and post-dose on Day 2 of each 3-day in-laboratory study period
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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.
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Pre-dose and post-dose on Day 2 of each 3-day in-laboratory study period
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Diastolic Blood Pressure Before and After Study Drug Administration
Časové okno: Pre-dose and post-dose on Day 2 of each 3-day in-laboratory study period
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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.
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Pre-dose and post-dose on Day 2 of each 3-day in-laboratory study period
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Proportion of Required Blood Samples Collected
Časové okno: Through completion of the second 3-night in-laboratory study period
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Proportion of protocol-specified blood samples successfully collected during the in-laboratory study periods.
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Through completion of the second 3-night in-laboratory study period
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Number of Participants Unable to Complete a Study Procedure Due to Intolerance
Časové okno: From enrollment through completion of the 10-day ambulatory follow-up following the second study period
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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.
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From enrollment through completion of the 10-day ambulatory follow-up following the second study period
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Proportion of Required Core Body Temperature Capsule Assessments Completed
Časové okno: Pre-laboratory Day 6, continuously during the 3-day in-laboratory protocol, and post-laboratory Days 4 and 6 during each study period
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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.
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Pre-laboratory Day 6, continuously during the 3-day in-laboratory protocol, and post-laboratory Days 4 and 6 during each study period
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Proportion of Participants Adherent to Required Caffeine Restrictions
Časové okno: From 72 hours before admission through completion of the 3-night in-laboratory protocol during each study period
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Proportion of participants who adhere to protocol-specified caffeine restrictions during required study monitoring periods.
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From 72 hours before admission through completion of the 3-night in-laboratory protocol during each study period
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Proportion of Participants Adherent to Required Alcohol Restrictions
Časové okno: From 24 hours before admission through completion of the 3-night in-laboratory protocol during each study period
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Proportion of participants who adhere to protocol-specified alcohol restrictions during required study monitoring periods.
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From 24 hours before admission through completion of the 3-night in-laboratory protocol during each study period
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Sekundární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
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Dim Light Melatonin Onset (DLMO) timing
Časové okno: During the 3-hour dim-light period preceding habitual bedtime on each in-laboratory study day
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Circadian phase assessed using dim light melatonin onset derived from serial plasma melatonin sampling during controlled dim-light conditions.
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During the 3-hour dim-light period preceding habitual bedtime on each in-laboratory study day
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Sleep Latency Measured by Polysomnography
Časové okno: Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Sleep latency, defined as the time from lights out to sleep onset, measured by overnight polysomnography.
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Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Total Sleep Time Measured by Polysomnography
Časové okno: Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Total time spent asleep during the overnight sleep period, measured by polysomnography and reported in minutes.
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Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Sleep Efficiency Measured by Polysomnography
Časové okno: Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Sleep efficiency measured by polysomnography, calculated as total sleep time divided by time in bed multiplied by 100 and reported as a percentage.
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Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Wake After Sleep Onset Measured by Polysomnography
Časové okno: Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Total time spent awake after initial sleep onset and before final awakening, measured by polysomnography and reported in minutes.
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Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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REM Sleep Latency Measured by Polysomnography
Časové okno: Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Time from sleep onset to the first epoch of rapid eye movement (REM) sleep, measured by polysomnography and reported in minutes.
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Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Percentage of Total Sleep Time Spent in N2 Sleep Measured by Polysomnography
Časové okno: Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Percentage of total sleep time classified as stage N2 sleep based on polysomnography.
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Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Percentage of Total Sleep Time Spent in N3 Sleep Measured by Polysomnography
Časové okno: Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Percentage of total sleep time classified as stage N3 sleep based on polysomnography.
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Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Percentage of Total Sleep Time Spent in REM Sleep Measured by Polysomnography
Časové okno: Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Percentage of total sleep time classified as rapid eye movement (REM) sleep based on polysomnography.
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Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Phase of the Core Body Temperature Circadian Rhythm
Časové okno: Continuously across the 3-day in-laboratory protocol during each study period
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Circadian phase of the core body temperature rhythm derived from continuous core body temperature monitoring using a rectal thermistor
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Continuously across the 3-day in-laboratory protocol during each study period
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Amplitude of the Core Body Temperature Circadian Rhythm
Časové okno: Continuously across the 3-day in-laboratory protocol during each study period
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Amplitude of the core body temperature rhythm derived from continuous core body temperature monitoring using a rectal thermistor.
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Continuously across the 3-day in-laboratory protocol during each study period
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Amplitude of the Melatonin Rhythm
Časové okno: Across the 3-day in-laboratory protocol during each study period
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Amplitude of the melatonin rhythm derived from serial plasma melatonin concentrations collected under controlled in-laboratory conditions.
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Across the 3-day in-laboratory protocol during each study period
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EEG Delta Oscillation Power
Časové okno: Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Delta-band EEG power derived from quantitative EEG spectral analysis during overnight polysomnography and reported in squared microvolts (µV²).
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Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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EEG Delta Oscillation Power Density
Časové okno: Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Delta-band EEG power spectral density derived from quantitative EEG spectral analysis during overnight polysomnography and reported in squared microvolts per hertz (µV²/Hz).
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Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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EEG Slow Oscillation Power
Časové okno: Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Slow-oscillation EEG power derived from quantitative EEG spectral analysis during overnight polysomnography and reported in squared microvolts (µV²).
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Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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EEG Theta Oscillation Power
Časové okno: Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Theta-band EEG power derived from quantitative EEG spectral analysis during overnight polysomnography and reported in squared microvolts (µV²).
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Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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EEG Alpha Oscillation Power
Časové okno: Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Alpha-band EEG power derived from quantitative EEG spectral analysis during overnight polysomnography and reported in squared microvolts (µV²).
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Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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EEG Beta Oscillation Power
Časové okno: Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Beta-band EEG power derived from quantitative EEG spectral analysis during overnight polysomnography and reported in squared microvolts (µV²).
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Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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EEG Sigma Oscillation Power During NREM Sleep
Časové okno: Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Sigma-band EEG power derived from quantitative EEG spectral analysis during non-rapid eye movement (NREM) sleep stages and reported in squared microvolts (µV²).
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Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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EEG Slow-Wave Amplitude
Časové okno: Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Mean amplitude of detected EEG slow waves derived from quantitative EEG analysis during overnight polysomnography and reported in microvolts (µV).
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Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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EEG Slow-Wave Slope
Časové okno: Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Mean slope of detected EEG slow waves derived from quantitative EEG analysis during overnight polysomnography and reported in microvolts per second (µV/s).
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Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Sleep Spindle Density During NREM Sleep
Časové okno: Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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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.
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Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Sleep Spindle Frequency During NREM Sleep
Časové okno: Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Mean frequency of detected sleep spindles derived from quantitative EEG analysis during non-rapid eye movement (NREM) sleep stages and reported in hertz (Hz).
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Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Sleep Spindle Duration During NREM Sleep
Časové okno: Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Mean duration of detected sleep spindles derived from quantitative EEG analysis during non-rapid eye movement (NREM) sleep stages and reported in seconds.
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Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Sleep Spindle Amplitude During NREM Sleep
Časové okno: Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Mean amplitude of detected sleep spindles derived from quantitative EEG analysis during non-rapid eye movement (NREM) sleep stages and reported in microvolts (µV).
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Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Time Spent in N1 Sleep Measured by Polysomnography
Časové okno: Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Total time classified as stage N1 sleep based on polysomnography and reported in minutes.
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Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Time Spent in N2 Sleep Measured by Polysomnography
Časové okno: Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Total time classified as stage N2 sleep based on polysomnography and reported in minutes.
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Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Time Spent in N3 Sleep Measured by Polysomnography
Časové okno: Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Total time classified as stage N3 (slow-wave) sleep based on polysomnography and reported in minutes.
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Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Time Spent in REM Sleep Measured by Polysomnography
Časové okno: Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Total time classified as rapid eye movement (REM) sleep based on polysomnography and reported in minutes.
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Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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EEG Slow-Wave Density
Časové okno: Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Density of detected EEG slow waves derived from quantitative EEG analysis during overnight polysomnography and reported as the number of slow waves per minute.
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Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Percentage of Total Sleep Time Spent in N1 Sleep Measured by Polysomnography
Časové okno: Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Percentage of total sleep time classified as stage N1 sleep based on polysomnography.
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Each night (Nights 1, 2, and 3) of each 3-night in-laboratory study period
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Další výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
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Plasma p-tau217 Concentrations Across the 24-Hour Sleep-Wake Cycle
Časové okno: Across the 24-hour sleep-wake cycle during each in-laboratory study period
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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.
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Across the 24-hour sleep-wake cycle during each in-laboratory study period
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Sleep Onset Time Measured by Wrist Actigraphy
Časové okno: Days 1-7 of the pre-laboratory monitoring period and Days 1-10 of the post-laboratory ambulatory monitoring period during each study period
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Sleep onset time derived from wrist-worn actigraphy during ambulatory monitoring.
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Days 1-7 of the pre-laboratory monitoring period and Days 1-10 of the post-laboratory ambulatory monitoring period during each study period
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Total Sleep Time Measured by Wrist Actigraphy
Časové okno: Days 1-7 of the pre-laboratory monitoring period and Days 1-10 of the post-laboratory ambulatory monitoring period during each study period
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Total sleep time derived from wrist-worn actigraphy during ambulatory monitoring and reported in minutes.
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Days 1-7 of the pre-laboratory monitoring period and Days 1-10 of the post-laboratory ambulatory monitoring period during each study period
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Sleep Fragmentation Index Measured by Wrist Actigraphy
Časové okno: 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
Časové okno: 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
Časové okno: 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
Časové okno: 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
Časové okno: 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
Časové okno: 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
Časové okno: 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
Časové okno: 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
Časové okno: 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
Časové okno: 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
Časové okno: 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
Časové okno: 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
Časové okno: 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
Časové okno: 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
|
Spolupracovníci a vyšetřovatelé
Sponzor
Spolupracovníci
Termíny studijních záznamů
Hlavní termíny studia
Začátek studia (Odhadovaný)
Primární dokončení (Odhadovaný)
Dokončení studie (Odhadovaný)
Termíny zápisu do studia
První předloženo
První předloženo, které splnilo kritéria kontroly kvality
První zveřejněno (Aktuální)
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Aktuální)
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
Naposledy ověřeno
Více informací
Termíny související s touto studií
Klíčová slova
Další identifikační čísla studie
- 2026P001362
Plán pro data jednotlivých účastníků (IPD)
Plánujete sdílet data jednotlivých účastníků (IPD)?
Popis plánu IPD
Časový rámec sdílení IPD
Kritéria přístupu pro sdílení IPD
Typ podpůrných informací pro sdílení IPD
- PROTOKOL STUDY
- MÍZA
Informace o lécích a zařízeních, studijní dokumenty
Studuje lékový produkt regulovaný americkým FDA
Studuje produkt zařízení regulovaný americkým úřadem FDA
produkt vyrobený a vyvážený z USA
Tyto informace byly beze změn načteny přímo z webu clinicaltrials.gov. Máte-li jakékoli požadavky na změnu, odstranění nebo aktualizaci podrobností studie, kontaktujte prosím register@clinicaltrials.gov. Jakmile bude změna implementována na clinicaltrials.gov, bude automaticky aktualizována i na našem webu .