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Clinical Trial Summary

Mechanical ventilation is a widely used treatment on the Intensive Care Unit (ICU). Swallowing dysfunction (dysphagia) after extubation may cause aspiration, and is associated with poor outcomes: pneumonia, reintubation, a prolonged length of hospital stay and increased mortality. The exact underlying pathophysiology of post-extubation dysphagia (PED) is unknown. This exploratory pilot study is the first step that aims to fill this knowledge gap to ultimately improve current treatment and prevention of post-extubation dysphagia. Using FEES (Flexible Endoscopic Evaluation of Swallowing), HRIM (High Resolution Impedance Manometry) and EMG (electromyography) simultaneously, 5 healthy subjects and 25 patients within 24 hours after extubation will be studied.


Clinical Trial Description

Observational study model: The group of healthy subjects will be recruited using posters at the local university and the internet. The healthy subjects will be studied before the group of patients to assess the feasibility and possible interactions of simultaneously recording FEES, HRIM and EMG. Then, the group of patients will be studied. They will be recruited from the Intensive Care Unit. See In- and Exclusion criteria for details. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03761823
Study type Observational
Source Radboud University Medical Center
Contact
Status Terminated
Phase
Start date January 22, 2019
Completion date February 28, 2019

See also
  Status Clinical Trial Phase
Recruiting NCT06386159 - Clinical Application of Comprehensive Intervention for PED Based on Neuroregulatory Mechanism N/A