Actively Recruiting

All Genders
NCT01195558

Patient Registry of Blind Subjects With Sleep-related Problems

Led by Vanda Pharmaceuticals · Updated on 2020-06-24

10000

Participants Needed

1

Research Sites

1043 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Non-24-hour sleep-wake disorder (Non-24) is a condition experienced primarily by totally blind individuals that results in abnormal night sleep patterns and chronic daytime sleepiness. This is a research protocol to develop a patient registry of subjects who may suffer from Non-24 and who are blind. Subjects participate in the study through a phone survey. This registry will be used to better understand, sleep related problems in blind individuals, including the investigation of a potential treatment, recruitment for future clinical studies, and to provide a forum for raising awareness about Non-24. The survey consists of questions regarding the degree of vision impairment and sleep problems that the subjects may be experiencing.

CONDITIONS

Official Title

Patient Registry of Blind Subjects With Sleep-related Problems

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Subjects or legal guardians must be at least 18 years of age to participate in the telephone survey. Parents or legal guardians may represent children from 0 through 17 years who meet the following criteria.
  • Subjects must be blind.
  • Subjects must have some self-described problem with sleep or daytime sleepiness.
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

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Trial Site Locations

Total: 1 location

1

Vanda Pharmaceuticals

Washington D.C., District of Columbia, United States, 20037

Actively Recruiting

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Research Team

V

Vanda Pharmaceuticals

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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