Ventilation volume efficacy via nasal and oral airway during induction of anesthesia

Ventilation volume efficacy via nasal and oral airway during induction of anesthesia - Ventilation volume efficacy via nasal and oral airway

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000022184

Enrollment

Registered

2016-05-02

Start date

2016-05-06

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

Patient who undergo general anesthesia with rapid induction

Interventions

Evaluation of1 total 2 oral3 nasal ventilation volume Evaluation of1 total2 nasal 3 oral ventilation volume

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients who undergo general anesthesia wirh rapid induction.

Exclusion criteria

Exclusion criteria: Anticipated mask ventilation difficulty GER patients

Design outcomes

Primary

Measure	Time frame
Mask ventilation efficacy such as ventilation volume or ITP.	—

Secondary

Measure	Time frame
Subjective difficulty of mask ventilation	—

Countries

Japan

Contacts

Public ContactNobuyasu Komasawa

Osaka Medical College Anesthesiology

ane078@poh.osaka-med.ac.jp0726-84-6361

Outcome results

None listed

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