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Clinical Trial Summary

Oculopharyngeal muscular dystrophy (OPMD) is a rare myopathic disease that results in progressive degeneration of the oral and pharyngeal muscular, resulting in severe dysphagia and dysarthria. OPMD is considered a rare disease; therefore, limited research is available on the natural progression of the disease or the utility of biomarkers to identify swallowing impairment. The aim of this study is:

1. To identify accurate, reliable and non-invasive clinical markers of swallowing impairment

2. To determine the discriminate ability of these markers to identify impairments in swallow safety and swallowing efficiency.


Clinical Trial Description

Participants will be recruited from the Neurology clinic at the University of Florida. The single evaluation will occur in the PIs research laboratory at the University of Florida, Gainesville, Florida. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02877784
Study type Observational
Source University of Florida
Contact
Status Completed
Phase
Start date October 2016
Completion date August 2017

See also
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Enrolling by invitation NCT04009408 - Expiratory Muscle Strength Training (EMST) in Neuromuscular Disorders N/A
Recruiting NCT03874910 - Pathology Analysis of OPMD Patient Myotomies
Withdrawn NCT04226924 - Treatment of Oculopharyngeal Muscular Dystrophy With Trehalose Phase 2
Recruiting NCT02158156 - Effect of Aerobic Training in Patients With Oculopharyngeal Muscular Dystrophy N/A
Completed NCT02015481 - Safety Tolerability and Efficacy Study of Cabaletta to Treat Oculopharyngeal Muscular Dystrophy (OPMD) Patients Phase 2
Withdrawn NCT03161847 - Natural History Study of Oculopharyngeal Muscular Dystrophy