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High-flow nasal cannula therapy for acute exacerbation of chronic obstructive pulmonary disease patients with type II respiratory failure

High-flow nasal cannula therapy for acute exacerbation of chronic obstructive pulmonary disease patients with type II respiratory failure

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600123567
Enrollment
Unknown
Registered
2026-04-28
Start date
2026-05-01
Completion date
Unknown
Last updated
2026-05-04

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

Conditions

Chronic obstructive pulmonary disease, COPD

Interventions

HFNC group:HFNC Treatment
NIV group:Noninvasive ventilation (NIV) was used

Sponsors

Affiliated Hospital of Jiangnan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Meets the diagnostic criteria for acute exacerbation of chronic obstructive pulmonary disease (AECOPD) accompanied by type II respiratory failure; (2) The clinical condition cannot be improved by relying solely on low-flow nasal cannula oxygen inhalation; (3) Age range: 18 - 80 years old, gender not restricted; (4) Voluntary to receive treatment and sign the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Patients with airflow limitation caused by asthma, bronchiectasis, or pulmonary fibrosis; (2) Those who have undergone lung transplantation or lung resection; (3) Those with severe hypertension, heart failure, arrhythmia, diabetes, primary heart, liver, kidney, blood, or neurological symptoms that are poorly controlled; (4) Patients with lung tumors, malignant tumors (within <5 years from the initial diagnosis, or with recurrence or metastasis confirmed by imaging or tumor markers, or undergoing radiotherapy, chemotherapy, targeted therapy, or immunotherapy, etc.); (5) Pregnant women, women planning to conceive, or lactating women; (6) Patients considered ineligible by the researchers.

Design outcomes

Primary

MeasureTime frame
Blood gas analysis;Chest CT;

Secondary

MeasureTime frame
Sputum culture;Blood inflammatory indicators, liver and kidney functions, myocardial enzymes, etc.;Pulmonary function;

Countries

China

Contacts

Public ContactZuo Zhitong

Affiliated Hospital of Jiangnan University

zzt555@163.com+86 15301516370

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 7, 2026