High Flow Nasal Cannula vs NPPV in Moderate Chronic Obstructive Pulmonary Disease Exacerbation
Recruiting in Palo Alto (17 mi)
Overseen ByQingyuan Zhan, M.D.
Age: 18+
Sex: Any
Travel: May Be Covered
Time Reimbursement: Varies
Trial Phase: Academic
Waitlist Available
Sponsor: China-Japan Friendship Hospital
No Placebo Group
Trial Summary
What is the purpose of this trial?For moderate AECOPD(pH\<7.35), several guidelines have strongly recommended NPPV as standard therapy, which can reduce the rate of intubation and mortality. A few previous studies have shown that HFNC can efficiently improve alveoli ventilation and breathing pattern in some severe AECOPD patients. Therefore, we hypothesize that HFNC is not inferior to NPPV for preventing endotracheal intubation in moderate AECOPD patients. To assess this hypothesis, we performed a multicenter, randomized, noninferiority trial of HFNV vs NPPV in moderate AECOPD patients.
Eligibility Criteria
Inclusion Criteria
AECOPD; 7.35>pH≥7.25,PaCO2>50 mmHg
Participant Groups
2Treatment groups
Experimental Treatment
Active Control
Group I: High flow nasal cannulaExperimental Treatment1 Intervention
High flow nasal cannula(OptiflowTM); Flow 25-60 L/min is set according to patients' comfort; FiO2 is adjusted to maintain peripheral capillary oxygen saturation(SpO2) 90-95%; temperature is set at 37 degree centigrade.
Group II: Noninvasive positive ventilationActive Control1 Intervention
Parameters are set according to NPPV protocols
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Who Is Running the Clinical Trial?
China-Japan Friendship HospitalLead Sponsor