Detection of aspiration risk using near-infrared fluorescent clinical test system
Not Applicable
Recruiting
- Conditions
- dysphasia
- Registration Number
- JPRN-UMIN000040116
- Lead Sponsor
- Tokyo Medical and Dental University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
Not provided
Exclusion Criteria
subjects those cannot perform VF due to allergy of contrast medium or gastrointestinal disease subject who do not agree to participate the study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Methods 1.Detection of pharyngeal residue by using near-infrared fluorescent clinical test system 2.Assessment of swallowing function by VE and VF The results obtained from each test are compared and the usefulness of the near-infrared fluorescence clinical test system is verified.
- Secondary Outcome Measures
Name Time Method