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