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New Method of Oxygen Delivery System to Relieve Patients Discomfort

New Method of Oxygen Delivery System to Relieve Patients Discomfort

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0001164
Enrollment
10
Registered
2014-07-14
Start date
2013-02-05
Completion date
Unknown
Last updated
2019-03-11

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

Conditions

None listed

Interventions

None listed

Sponsors

Asan Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: - Over 20 years old - Either hospitalization at pulmonary ward or Out Patient Department follow up patient who needs oxygen supply due to hypoxia caused by COPD, Asthma, Pneumonia, Diffuse Interstitial Lung Disease - Using nasal prong system - Range of oxygen supply is from 1L to 4L per minute at enrollment point

Exclusion criteria

Exclusion criteria: - Unable to maintain over 90% of saturation with nasal prong system - Unstable Blood Pressure (BP), Pulse Rate (PR), and so on - Who has transmitted disease such as Tuberculosis (TB), Respiratory Syncytial Virus (RSV), Parainfluenza virus, Mycoplasma - Subject declines the participation

Design outcomes

Primary

MeasureTime frame
Discomfort Visual Analogue Sclae (Discomfort VAS)

Secondary

MeasureTime frame
Saturation by pulse oxymetry (SpO2)

Countries

Korea, Republic of

Contacts

Public ContactSei Won Lee

Asan Medical Center

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026