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Improving the Assessment of Hypersomnolence

NCT02884505 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 132

Last updated 2019-08-22

No results posted yet for this study

Summary

The overall purpose of this study is to employ a pragmatic, multidimensional assessment of hypersomnolence that "piggybacks" on routine clinical care in patients with suspected disorders of central nervous system (CNS) hypersomnia, to determine whether these additional objective and subjective assessments are useful in the diagnosis and management of these patients.

Conditions

  • Disorders of Excessive Somnolence

Interventions

DEVICE

Pupillometry

Measures pupillary dynamics in darkness and light conditions

BEHAVIORAL

Psychomotor Vigilance Task

Response time task measuring neurobehavioral alertness

OTHER

Auditory Evoked Potential

Measure of electroencephalographic response to standardized auditory tones

BEHAVIORAL

Hypersomnia Severity Index

Self-report measure of hypersomnolence

Sponsors & Collaborators

  • University of Wisconsin, Madison

    lead OTHER

Principal Investigators

  • David T Plante, MD · University of Wisconsin, Madison

Eligibility

Min Age
18 Years
Max Age
89 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-08-25
Primary Completion
2019-06-30
Completion
2019-06-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02884505 on ClinicalTrials.gov