Closed Loop Oxygen Control in Chronic Obstructive Pulmonary Disease (COPD) Patients Treated With Nasal High Flow in the Hospital

ConditionCOPD
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age22+
SponsorFisher and Paykel Healthcare

About this trial

The trial aims to evaluate whether the Airvo 3 device in OptiO2 mode can maintain patients' SpO2 levels within the target range better than manual oxygen titration in hospitalized COPD patients with hypoxemia/respiratory distress.

Eligibility criteria

Qualifiers

Has cognitive ability to provide informed consent

Aged 22 years or older

Hospitalized with hypoxemia/respiratory distress

Diagnosis of COPD

Disqualifiers

Receiving Non Invasive Ventilation (NIV) or indicated for NIV as per European Respiratory Society /American Thoracic Society guidelines

Hemodynamic instability (systolic blood pressure <90mmHg or requirement for vasopressor or inotropic support)

Patient receiving end of life care

Nasal or facial conditions precluding use of nasal high flow

Trial design

Treatments tested in this trial

  • Closed loop oxygen control
  • Manual titration

Treatment groups

70 Participants
are divided into 2 treatment groups

Sponsors and collaborators