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Examination of adequacy of swallowing larynx distance estimated by NESSiE automatic evaluation program - Comparison with manual measurement from videofluoroscopic examination of swallowing-

Examination of adequacy of swallowing larynx distance estimated by NESSiE automatic evaluation program - Comparison with manual measurement from videofluoroscopic examination of swallowing- - Examination of adequacy of swallowing larynx distance estimated by NESSiE automatic evaluation program - Comparison with manual measurement from videofluoroscopic examination of swallowing-

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000032755
Enrollment
12
Registered
2018-07-18
Start date
2018-07-17
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

dysphagia

Interventions

None listed

Sponsors

National Center for Global Health and Medicine
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: Healthy adult male

Exclusion criteria

Exclusion criteria: 1) Persons who are allergic to X-ray contrast medium (barium sulfate) 2) Persons who have judged that the research director is inappropriate for inclusion in research

Design outcomes

Primary

MeasureTime frame
Laryngeal elevation distance

Secondary

MeasureTime frame
Laryngeal elevation time

Countries

Japan

Contacts

Public ContactJunko Fujitani

National Center for Global Health and Medicine department of rehabilitation medicine

jufujita@hosp.ncgm.go.jp0332027181

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026