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Prediction of aspiration using pharyngeal width taken during VFSS

Prediction of aspiration using pharyngeal width taken during VFSS

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0002352
Enrollment
300
Registered
2017-06-12
Start date
2017-06-01
Completion date
Unknown
Last updated
2019-03-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

None listed

Sponsors

Hallym University Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: - Experimental group 1.Patients aged 20 or above 2.Conscious patients in an alert state 3.Patients, who can keep sitting down during the videofluoroscopic swallowing study (for about 3 to 5 minutes) 4.Patients, who agree with the study - Control group 1.People aged 20 or above 2.Consciouspeople in an alert state 3.People with no swallowing disorders 4.People with no stroke, degenerative brain diseases, head and neck cancers and experience in receiving brain and laryngeal surgery 5.People, who can keep sitting down durng the videofluoroscopic swallowing for about 3 to 5 minutes) 6.People, who agree with the study

Exclusion criteria

Exclusion criteria: 1.Conscious patients below an alert state 2.Patients, who may have bedsores around the hip worsened when they keep sitting down

Design outcomes

Primary

MeasureTime frame
Pharyngeal width

Secondary

MeasureTime frame
Penetration-Aspiration scale

Countries

Korea, Republic of

Contacts

Public ContactJUNG IL HWAN

Hallym University

died45@naver.com+82-31-380-3860

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026