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Development of Clinical Database of Individuals With Smith-Magenis Syndrome and Sleep Disturbances

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Vanda Pharmaceuticals

Status

Enrolling

Conditions

Sleep Disturbances in Smith-Magenis Syndrome

Treatments

Other: Data collection of sleep disturbances in individuals with SMS

Study type

Observational

Funder types

Industry

Identifiers

NCT03154697
Pro00015678

Details and patient eligibility

About

This database will be used to better understand the sleep problems of people with SMS. This clinical database will be a part of a larger Smith-Magenis Patient Registry used to create an awareness campaign around SMS and the sleep disturbances that are characteristic of the disorder.

Enrollment

1,000 estimated patients

Sex

All

Ages

3 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Parent or legal guardian of individual with Smith-Magenis Syndrome

Exclusion criteria

  • Not legal guardian of individual with SMS

Trial contacts and locations

1

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Central trial contact

Vanda Pharmaceuticals

Data sourced from clinicaltrials.gov

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