Status:
TERMINATED
Automated Adjustment of Oxygen on Patient With Acute COPD Exacerbation - FreeO2 HypHop
Lead Sponsor:
Laval University
Conditions:
Oxygen Toxicity
COPD Exacerbation
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The aim of this study is to evaluate if automated adjustment of oxygen (with FreeO2 device) can reduce the hospital length of stay for acute exacerbation of COPD with comparison of manual oxygen titra...
Detailed Description
The aim of this study is to evaluate if automated adjustment of oxygen (with FreeO2 device) can reduce the hospital length of stay for acute exacerbation of COPD with comparison of manual oxygen titra...
Eligibility Criteria
Inclusion
- COPD or suspected COPD ( Age\>40, active or smoking history \> 10pack/years), -
- Acute exacerbation (increasing dyspnea recently)
- One or more of the following criteria: increased sputum, modification of sputum purulence,increased dyspnea,
- Moderate oxygen therapy: Oxygen flow \< 8 lpm (or FiO2 \< 0.60) to maintain a SpO2 \>or = 92% (for long term oxygen therapy, the oxygen flow must be greater than baseline flow to maintain SpO2 \> or = 92%)
Exclusion
- Patient refusal
- COPD exacerbation with diagnosis highly related to pulmonary embolism, cardiac pulmonary edema, pneumothorax or sedative overdose
- No SpO2 signal
- Encephalopathy score \> 2
- Delirium
- Other respiratory support needed (intubation or NIV)
- Patient on withdrawal life support
- Advance neoplasia (palliative stage) or terminal respiratory distress
- Unavailability of FreeO2 device at the randomisation
- Non optimal patient collaboration
Key Trial Info
Start Date :
December 17 2018
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 12 2024
Estimated Enrollment :
17 Patients enrolled
Trial Details
Trial ID
NCT03835741
Start Date
December 17 2018
End Date
July 12 2024
Last Update
September 4 2025
Active Locations (1)
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1
Institut Universitaire de Cardiologie et de Pneumologie de Québec
Québec, Quebec, Canada, G1V4G5