Creating a database to understand sleep issues in Smith-Magenis Syndrome

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to develop a clinical database focused on the sleep disturbances experienced by individuals with Smith-Magenis Syndrome (SMS). The data collected will contribute to a larger patient registry that seeks to raise awareness about SMS and its associated sleep problems. By gathering detailed information from parents or legal guardians of affected individuals, the study will help identify patterns and potential interventions for managing sleep disturbances in this population.

Why it matters

Who can join: the full rules

Inclusion Criteria:

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

Exclusion Criteria:

* Not legal guardian of individual with SMS

Where it's running

• Vanda Pharmaceuticals
  Washington D.C., District of Columbia, United States Recruiting

Study contacts

• Study coordinator: Vanda Pharmaceuticals
• Email: clinicaltrials@vandapharma.com
• Phone: 202-734-3400

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.