An Observational Study to Investigate the Effects of Rapid Transmeridian Travel
NCT ID: NCT02560103
Last Updated: 2018-06-26
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
119 participants
OBSERVATIONAL
2015-09-30
2017-10-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Circadian Rhythm Disruption in the Hospital Intensive Care Environment
NCT05828680
Influence of Sleep Regularity on Circadian Rhythms, Learning, Performance, and Mood
NCT02839070
The Effect of a Continuous 1-Hour Time Delay on Circadian Rhythms
NCT07317349
Comparison Across Multiple Types of Sleep Deprivation
NCT04211506
Age-related Changes in Sleep-wake Regulation
NCT03813082
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_ONLY
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Single group
No treatment
Transmeridian travel across multiple time zones
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Transmeridian travel across multiple time zones
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Men or women between 18-75 years
* Body Mass Index of ≥ 18 and ≤ 30 kg/m2
Exclusion Criteria
* Major surgery, trauma, illness or immobile for 3 or more days within the past month
* Pregnancy or recent pregnancy (within 6 weeks)
* A positive test for drugs of abuse at the screening visit
* Any other sound medical reason as determined by the clinical investigator
18 Years
75 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Vanda Pharmaceuticals
INDUSTRY
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Santa Monica Clinical Trials
Santa Monica, California, United States
The Center for Sleep & Wake Disorders
Chevy Chase, Maryland, United States
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
VP-VEC-162-0101
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.