STARD 2015: an updated list of essential items for reporting diagnostic accuracy studies.
Patrick M Bossuyt, Johannes B Reitsma, David E Bruns...
https://pubmed.ncbi.nlm.nih.gov/26511519/Actively Recruiting
Led by University Hospital, Grenoble · Updated on 2026-04-15
240
Participants Needed
2
Research Sites
13 weeks
Total Duration
Chronic obstructive pulmonary disease COPD is a common and serious lung condition affecting 8 to 12% of adults and is a leading cause of death in developed countries. This research investigates the use of end-tidal carbon dioxide EtCO2, a non-invasive measurement, to predict severe COPD exacerbations and estimate arterial carbon dioxide levels without the need for blood sampling. Early detection of exacerbations is important to improve patient survival. In this observational study conducted in emergency departments, patients admitted with acute COPD exacerbations will have their EtCO2 levels measured by nurses using a mask or oxygen glasses at the time of initial assessment. Treatment will follow current international guidelines, and the doctors will not see the EtCO2 results. Researchers will then track whether patients require invasive or non-invasive ventilation within the first 24 hours after admission. Participants will be monitored during their emergency department stay, with clinical data collected from medical records 24 hours after admission. Additional measures include arterial blood gas tests taken about 15 minutes after arrival to compare EtCO2 readings with blood carbon dioxide levels. The study focuses on how well EtCO2 predicts the need for ventilation support and its agreement with standard blood gas measurements, helping to improve assessment and treatment of COPD flare-ups.
CONDITIONS
Monitoring of the End-tidal Carbon Dioxide (EtCO2) as a Severity Criterion in COPD Exacerbations
N
Nicolas SEGOND, MD
P
Prudence MABIALA MAKELE, PhD
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University Hospital, Grenoble
Lead Sponsor
Hospices Civils de Lyon
Collaborating Sponsor
You may qualify if you...
You will not qualify if you...
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person) at emergency department reception
Duration - Within 15 minutes after emergency admission
Participants undergo measurement of end-tidal carbon dioxide (EtCO2) during vital sign assessment at emergency department reception using a mask or oxygen glasses. Additional arterial blood gas measurements occur shortly after admission.
1 visit (in-person) at emergency department
Duration - 24 hours after admission
Participants are observed after discharge from the emergency department with clinical outcomes collected 24 hours after admission from medical records.
No additional visits; data collected from medical records
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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https://pubmed.ncbi.nlm.nih.gov/19931750/University Hospital, Grenoble
Lead Sponsor
Hospices Civils de Lyon
Collaborating Sponsor