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Feasibility of a Water-soluble Contrast Application Into Dysphagia Evaluation

Dysphagia Clinical Trial

Official title:
Feasibility of a Water-soluble Contrast Application Into Dysphagia Evaluation

Clinical Trial Summary

In traditional video-fluoroscopic-swallowing study, a lipid-soluble contrast (barium sulfate) has been used more than 30 years. However, it can cause chemical pneumonitis and subsequently impair reliability of video-fluoroscopic-swallowing study if aspirated. The authors reviewed the safety and usefulness of an water soluble agent-based swallowing test.

Clinical Trial Description

Parallel-group, case-controlled trial was conducted from September 2015 to November 2017. All the patients who referred for video-fluoroscopic-swallowing study were screened.

Based on the pre-emptive evaluation, high-risky patients were allocated to iohexol (Omnipaque)-used video-fluoroscopic-swallowing study and others were allocated to barium sulfate-used video-fluoroscopic-swallowing study.

Statistical Package for the Social Sciences 24 was used to perform statistical analysis for the data. Quantitative data were presented as mean ± standard errors. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03598491
Study type Observational
Source Ulsan University Hospital
Contact
Status Completed
Phase
Start date September 18, 2015
Completion date December 31, 2017
View Details
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