Capnography Monitoring in Ventilated Children
- Conditions
 - Infant, Newborn, DiseasesHeart Defects, CongenitalLung Diseases, InterstitialARDS, HumanChild, OnlyLung Diseases, ObstructiveCritical Illness
 
- Registration Number
 - NCT04354220
 
- Lead Sponsor
 - Vincenzo Cannizzaro
 
- Brief Summary
 End-tidal CO2 measurements in children will be assessed for their accuracy with arterial CO2 measurements.
- Detailed Description
 End-tidal and arterial CO2 measurements will be performed in invasively and non-invasively ventilated critically ill children. The endtidal CO2 values will assessed for their accuracy with respect to different underlying diseases and conditions of the children.
Recruitment & Eligibility
- Status
 - UNKNOWN
 
- Sex
 - All
 
- Target Recruitment
 - 178
 
- Children on pressure controlled mechanical invasive or non-invasive ventilation on the Paediatric Intensive Care Unit of the University Children's Hospital Zurich
 - Newborns with a birthweight of at least 2.0 kg
 - Newborns with an age of at least 1 hour (age > 60 minutes)
 - Children up to the last day of the 13th year of living
 - Ability of care taker or patient to understand verbal and written instructions and the general consent or informed consent in German or English
 - Obtained written general or informed consent as documented by signature
 - Available arterial line, i.e. a specific catheter inserted in an artery
 
- Care taker or participant unable for linguistic, mental or other reasons or unwilling to understand verbal or written information and to give written informed consent in German or English
 - Care taker not available
 - Newborns with a birthweight below 2.0 kg
 - Newborns younger than 1 hour (age <60 minutes)
 - Children with an age of 14 years onwards
 - Missing arterial line
 - Patients dependent on any other kind of respiratory support that is not compatible with the PcCO2-sensor or where a high leakage in the respiratory circuit makes PcCO2 measurements impossible (nasal mask ventilation, low-flow-/high-flow-ventilation, rebreathing mask, high- frequency-oscillation)
 - Patients where the investigators act on the assumption that mechanical ventilation will be discontinued and/or the arterial line will be removed within 6 hours or where only one pair of values (arterial and endtidal CO2) can be compared
 - Patients with a cyanotic shunt lesion with a weight of 15 kg or above
 
Study & Design
- Study Type
 - OBSERVATIONAL
 
- Study Design
 - Not specified
 
- Primary Outcome Measures
 Name Time Method Accuracy of end-tidal Carbon Dioxide (PetCO2) values in comparison to arterial Carbon Dioxide (PaCO2) values in invasively and non-invasively ventilated critically ill children without lung or heart disease On average every participant will be assessed for 5 days Mean absolute measurement difference between simultaneously obtained PaCO2 and PetCO2 values (bias) and their 95% limits of agreement (precision) in children and newborns without cardiopulmonary dysfunction. Units of measure will be in kilopascal (kPa) for PetCO2 and PaCO2, respectively.
- Secondary Outcome Measures
 Name Time Method Accuracy of end-tidal Carbon Dioxide (PetCO2) values in comparison to arterial Carbon Dioxide (PaCO2) values in invasively and non-invasively ventilated critically ill children with lung and or heart disease On average every participant will be assessed for 5 days Cardiopulmonary function-dependent mean absolute measurement difference between simultaneously obtained PaCO2 and PetCO2 values (bias) and their 95% limits of agreement (precision) in children and newborns with cardiopulmonary dysfunction. Units of measure will be in kilopascal (kPa) for PetCO2 and PaCO2, respectively.
Trial Locations
- Locations (1)
 University Children's Hospital
🇨🇭Zurich, Switzerland
University Children's Hospital🇨🇭Zurich, Switzerland
