Swallow sensor trial halted after failing to match gold standard
NCT ID NCT03387267
Summary
This study tested a new device called the Dysphagia Detection System (DDS), which is a small sensor worn on the neck. Researchers wanted to see if it could accurately detect unsafe or inefficient swallowing in people with conditions like stroke, Parkinson's, and dementia, compared to the standard X-ray test. The trial was stopped early because the device's performance did not meet the goals needed to continue.
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Contacts and locations
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Locations
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Boston Medical Center
Boston, Massachusetts, 02118, United States
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Helsinki University Central Hospital
Helsinki, 00029, Finland
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Henry Ford Health System
Detroit, Michigan, 48202, United States
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Kentucky Clinic
Lexington, Kentucky, 40536, United States
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Marionjoy Rehabilitation Hospital
Wheaton, Illinois, 60187, United States
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Medstar Rehabilitation Hospital
Washington D.C., District of Columbia, 20010, United States
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New York Presbyterian Hospital/Columbia University Medical Center
New York, New York, 10032, United States
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New York Presbyterian/Weill Cornell Medical Center
New York, New York, 10021, United States
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Rancho Research Institute, Rancho Los Amigos National Rehabilitation Center
Downey, California, 90242, United States
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Shirley Ryan AbilityLab
Chicago, Illinois, 60611, United States
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The Burke Medical Research Institute
White Plains, New York, 10605, United States
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The Cleveland Clinic Foundation
Cleveland, Ohio, 44195, United States
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University of Colorado Denver
Aurora, Colorado, 80045, United States
Conditions
Explore the condition pages connected to this study.