An Observational Study to Investigate the Effects of Rapid Transmeridian Travel

NCT ID: NCT02560103

Last Updated: 2018-06-26

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

119 participants

Study Classification

OBSERVATIONAL

Study Start Date

2015-09-30

Study Completion Date

2017-10-31

Brief Summary

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Observational study to investigate circadian rhythm patterns

Detailed Description

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Conditions

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Jet Lag Disorder

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Study Groups

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Single group

No treatment

Transmeridian travel across multiple time zones

Intervention Type OTHER

Interventions

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Transmeridian travel across multiple time zones

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Ability and acceptance to provide written consent
* Men or women between 18-75 years
* Body Mass Index of ≥ 18 and ≤ 30 kg/m2

Exclusion Criteria

* History (within the 12 months prior to screening) of psychiatric disorders
* 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
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Vanda Pharmaceuticals

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Santa Monica Clinical Trials

Santa Monica, California, United States

Site Status

The Center for Sleep & Wake Disorders

Chevy Chase, Maryland, United States

Site Status

Countries

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United States

Other Identifiers

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VP-VEC-162-0101

Identifier Type: -

Identifier Source: org_study_id

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