Clinical trials for decreasing work of breathing in Bi-flow system for healthy control

Status

Recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CRIS

Registry ID

KCT0006100

Enrollment

Registered

2021-04-27

Start date

2021-04-30

Completion date

Unknown

Last updated

2021-05-24

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

Conditions

None listed

Interventions

Medical Device : Total patients were devided into two groups, one group conducted a study with from a single flow(Uniflow) to Bi-flow, and the other group conducted a study with a Biflow to single flo

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: This study was an exploratory clinical trial and was selected healthy volunteers to confirm the effectiveness of the newly developed Bi-flow system from the existing HFNC.

Exclusion criteria

Exclusion criteria: Those who are unable to apply nasal cannula due to previous facial surgery, trauma, facial deformity, airway obstruction, etc. Patients with diseases that may interfere with this study, such as cardiovascular disease and lung diseases, which may affect daily life.

Design outcomes

Primary

Measure	Time frame
Work of breathing	—

Secondary

Measure	Time frame
changes in carbon dioxide in percutaneous, ventilation distribution, subjective acceptance of the patints	—

Countries

Korea, Republic of

Contacts

Public ContactWoo Jung Seo

Asan Medical Center

maoliang8874@gmail.com+82-2-3010-4710

Outcome results