Skip to content

Clinical study on the effect of a new nano polymer oxygen humidification membrane on oxygen therapy in patients with COPD

Clinical study on the effect of a new nano polymer oxygen humidification membrane on oxygen therapy in patients with COPD

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000036288
Enrollment
Unknown
Registered
2020-08-22
Start date
2020-10-01
Completion date
Unknown
Last updated
2020-09-07

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

Conditions

Chronic obstructive pulmonary disease

Interventions

Experimental group:Oxygen therapy with polymer oxygen humidification membrane
Control group:Oxygen therapy with ordinary oxygen humidification device

Sponsors

Shanghai General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged >= 18 years and <= 75 years, both male and female; 2. All patients met the diagnostic criteria of COPD in the gold guidelines 2020: after the application of bronchodilators, FEV1 / FVC < 70% indicated the existence of incomplete reversible airflow restriction. The percentage of FEV1 to the predicted value could be used to judge the degree of COPD airflow obstruction; 3. The symptoms of COPD patients were assessed according to the COPD assessment test (CAT) or the modified British Medical Research Council (MRC) dyspnea score. 4. Informed consent of patients.

Exclusion criteria

Exclusion criteria: 1. Patients with acute and chronic pain caused by lung cancer, pulmonary embolism, myocardial infarction, unstable angina pectoris, etc.; 2. Combined with bronchial asthma, pleural effusion or pneumatosis, heart failure and other sleep disorders; 3. Patients with sleep apnea syndrome or long-term use of hypnotic or sedative drugs; 4. Patients with anxiety, depression and mental system diseases, which affect communication and cognitive ability; 5. Patients with acute exacerbation complicated with respiratory failure were treated with ventilation; 6. The estimated survival time was less than 24 hours; 7. Pregnant or lactating patients.

Design outcomes

Primary

MeasureTime frame
The cumulative oxygen inhalation time (hours) was recorded by camera in 14 days.;

Secondary

MeasureTime frame
PaO2 within 14 days;Length of stay;Critical illness rate and first aid rate;

Countries

China

Contacts

Public ContactZhang Weixing

Shanghai General Hospital

monzwx@aliyun.com+86 13817657471

Outcome results

None listed

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