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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00001664
Other study ID # 970070
Secondary ID 97-N-0070
Status Completed
Phase N/A
First received November 3, 1999
Last updated June 30, 2017
Start date December 4, 1996
Est. completion date September 7, 2011

Study information

Verified date September 7, 2011
Source National Institutes of Health Clinical Center (CC)
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to assist training doctors about different diseases of the nervous system affecting sleep.

Patients selected to participate in this study will have any of a variety of sleep disorders. They will undergo several tests including an overnight recording of brain activity, eye movement, leg movement, breathing, heart rate, and other measures.

Results of these tests will be used to better understand diseases causing sleep disorders and may be used to develop better treatments for them.


Description:

The objective of this protocol is to provide training in a broad range of neurological sleep disorders to clinical associates who are eligible for sitting in the Board examination of the Added Qualification of Clinical Neurophysiology administered by the American Board of Psychiatry and Neurology. This protocol is to supplement small accrual of research patients who are referred from within the NIH.


Recruitment information / eligibility

Status Completed
Enrollment 83
Est. completion date September 7, 2011
Est. primary completion date
Accepts healthy volunteers No
Gender All
Age group 5 Years and older
Eligibility - IINCLUSION CRITERIA:

Patients 5 years of age and older, with the following referring diagnoses:

Narcolepsy

Hypersomnia

REM behavior disorder

Frontal nocturnal dystonia

Restless legs syndrome

Insomnia

Parasomnia

Nocturnal epileptic seizure

Nocturnal movement disorder

Sleep-related diagnostic dilemma

Sleep apnea associated with neurological disorders

Patients who are ambulatory and who are able to comply with the study procedures.

Patients who are able to understand and sign the informed consent. (Parent or guardian for minors).

EXCLUSION CRITERIA:

Patients who have been diagnosed with acute and progressive neurological disorders.

Patients who are unable to comply with the study procedures and require other than standard care.

Study Design


Locations

Country Name City State
United States National Institutes of Health Clinical Center, 9000 Rockville Pike Bethesda Maryland

Sponsors (1)

Lead Sponsor Collaborator
National Institute of Neurological Disorders and Stroke (NINDS)

Country where clinical trial is conducted

United States, 

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