Examination of airway management method in intravenous anesthesia using Nasal High Flow load device AIRVO

Examination of airway management method in intravenous anesthesia using Nasal High - Examination of airway management method in intravenous anesthesia using Nasal High Flow

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000038126

Enrollment

Registered

2019-10-09

Start date

2019-10-01

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

intravenous anesthesia

Interventions

propofol Dexmedetomidine

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Targeting healthy adult subjects (volunteers) who agree with the explanation of the contents of the research plan.

Exclusion criteria

Exclusion criteria: 1) Patients with severe respiratory illness 2) Patients with serious cardiovascular disease 3) Diabetes patients with poor control 4) Severe kidney injury patients 5) Patients with severe liver damage 6) Patients with hypersensitivity (allergy) to the drug to be used 7) Patients who are judged inappropriate by the research supervisor or research supervisor

Design outcomes

Primary

Measure	Time frame
Upper airway patency	—

Secondary

Measure	Time frame
Saliva swallowing function	—

Countries

Japan

Contacts

Public ContactTAKAO AYUSE

Nagasaki University Hospital Dental Anesthesia

ayuse@nagasaki-u.ac.jp0958197713

Outcome results

None listed

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