The assessment of the efficacy of Nasal High Flow System during sedation for the operation

The assessment of the efficacy of Nasal High Flow System during sedation for the operation - The efficacy of Nasal High Flow System during sedation for the operation

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000019697

Enrollment

Registered

2015-11-10

Start date

2015-11-10

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

patients who are sedated during the operation

Interventions

We use Nasal High Flow System in case which the respirational state becomes worse because of the sadation during the operation.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: patients whose state of respiration becomes worse because of the sadation during the operation patients who are able to provide written informed consent

Exclusion criteria

Exclusion criteria: patients who are judged inappropriate by the researchers

Design outcomes

Primary

Measure	Time frame
To assess the betterment of general or resperational state (apnea hypopnea index,oxygen saturation,body motion etc.)before and after the usage of Nasal High Flow System. We assess at the end of the usage of Nasal High Flow System.	—

Secondary

Measure	Time frame
To assess whether patients feel any inconvinience or not at the end of the operation	—

Countries

Japan

Contacts

Public ContactYoko Beppu

JCHO Osaka Hospital Department of Anesthesia

ysugimoto_0602@yahoo.co.jp06-6441-5451

Outcome results

None listed

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