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Purpose

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.

Condition

Eligibility

Eligible Ages
Between 3 Years and 65 Years
Eligible Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

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

Exclusion Criteria

  • Not legal guardian of individual with SMS

Study Design

Phase
Study Type
Observational
Observational Model
Case-Only
Time Perspective
Cross-Sectional

Recruiting Locations

Vanda Pharmaceuticals
Washington, District of Columbia 20037
Contact:
Vanda Pharmaceuticals
202-734-3400

More Details

NCT ID
NCT03154697
Status
Recruiting
Sponsor
Vanda Pharmaceuticals

Study Contact

Vanda Pharmaceuticals
202-734-3400
clinicaltrials@vandapharma.com

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.

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Vanderbilt University Medical Center