Status:

COMPLETED

Ultrasound and Videofluoroscopy for Diagnosing Swallowing Disorders

Lead Sponsor:

National Institutes of Health Clinical Center (CC)

Conditions:

Deglutition Disorder

Motor Neuron Disease

Eligibility:

All Genders

Brief Summary

This study will identify clinical signs and symptoms critical for diagnosing swallowing disorders and will characterize swallowing problems in various patient populations, such as patients with Parkin...

Detailed Description

Patients with neurological or neuromuscular conditions may be silent aspirators or at risk for laryngeal penetration or aspiration because of abnormal oropharyngeal functioning and thus are at risk fo...

Eligibility Criteria

INCLUSION CRITERIA:

Any Clinical Center inpatients and outpatients with known or suspected dysphagia on any other NIH institute protocol can be included for study as well as patients who are admitted specifically for this protocol.

Those patients at risk for oropharyngeal dysfunction will be screened initially by completing a self-assessment swallowing questionnaire, and by an interview with staff and/or family members. Patients who demonstrate appropriate signs and symptoms of dysphagia and oral motor impairment on the screening assessment will be considered for the protocol:

Difficulty swallowing food or pills.

Changed swallowing ability.

Coughing or choking when eating.

Shortness of breath during swallowing.

Food backing up into the mouth or nasal passage.

Fever or voice changes after swallowing.

Pain when swallowing.

Unexplained loss of weight.

EXCLUSION CRITERIA:

Patients who are severely demented or severely compromised will be excluded if they do not have sufficient cognitive ability to follow directions.

Patients who are non-ambulatory will be excluded if they can not be braced or supported within the fluoroscopy unit.

Highly agitated individuals will also be excluded if they are unable to remain confined in the equipment.

Infants and children under age 3 will be excluded due to radiation risk on the developing visual system.

Key Trial Info

Start Date :

October 1 1987

Trial Type :

OBSERVATIONAL

End Date :

November 1 2005

Estimated Enrollment :

750 Patients enrolled

Trial Details

Trial ID

NCT00001220

Start Date

October 1 1987

End Date

November 1 2005

Last Update

March 4 2008

Active Locations (1)

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1

National Institutes of Health Clinical Center (CC)

Bethesda, Maryland, United States, 20892