Status:
UNKNOWN
Capnography Monitoring in Ventilated Children
Lead Sponsor:
Vincenzo Cannizzaro
Conditions:
Child, Only
Infant, Newborn, Diseases
Eligibility:
All Genders
1-13 years
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 ...
Eligibility Criteria
Inclusion
- 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
Exclusion
- 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
Key Trial Info
Start Date :
June 9 2020
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
December 31 2023
Estimated Enrollment :
178 Patients enrolled
Trial Details
Trial ID
NCT04354220
Start Date
June 9 2020
End Date
December 31 2023
Last Update
May 18 2022
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
University Children's Hospital
Zurich, Switzerland, 8032