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Hypnotic Intake and Motor and Cognitive Performances at High Altitude

The Effect of Acute Hypnotic Intake Before a Night at High Altitude on Cognitive and Motor Performances

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02778659
Acronym
CHAM
Enrollment
22
Registered
2016-05-20
Start date
2016-05-31
Completion date
2017-10-31
Last updated
2018-01-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Physiology

Brief summary

This study aims to determine the effect of acute hypnotic intake (Zolpidem) on sleep, cognitive and motor performances and on acute mountain sickness symptoms at high altitude. Healthy subjects will be evaluated on 4 occasions (twice at sea level and twice at high altitude), after hypnotic or placebo intake. Following an early wake-up (01:00), symptoms, cognitive and motor performances will be assessed to determine potential residual effects of Zolpidem within such conditions.

Interventions

DRUGZolpidem

The hypnotic will be administrated orally at 22:00 in the evening before a sleep recording and an early wake-up at 01:00 for cognitive and motor assessment.

DRUGPlacebo

The placebo will be administrated orally at 22:00 in the evening before a sleep recording and an early wake-up at 01:00 for cognitive and motor assessment.

Sponsors

Centre d'Expertise sur l'Altitude EXALT
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* No sojourn above 2500 m during the past 2 months * Coffee intake \< 3 cups per day * Non-smoker

Exclusion criteria

* Respiratory, cardiovascular, metabolic or neuromuscular diseases * Psychiatric disorders * Use of hypnotics within the past year * Dependence syndrome (alcool, drugs, etc) * Severe insomnia or somnolence

Design outcomes

Primary

MeasureTime frameDescription
Cognitive performance assessed using Simon cognitive test4 hours after drug/placebo intakeSimon cognitive test

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026