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Evaluation of the clinical application of TcPCO2 measurements during rigid laryngoscopy or microlaryngeal surgery in childre

Completed
Conditions
Upper respiratory tract problems requiring surgery
10038716
Registration Number
NL-OMON50287
Lead Sponsor
Erasmus MC, Universitair Medisch Centrum Rotterdam
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
140
Inclusion Criteria

Patient is up to 18 years of age.
Indication to undergo a rigid laryngoscopic and/or microlaryngeal procedure.
Adequate end-tidal carbon dioxide measurements are unlikely during the planned
procedure.

Exclusion Criteria

Patient is older than 18 years of age
Procedure is carried out while patient is intubated.
Patient has a tracheal canula

Study & Design

Study Type
Observational non invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>The main study endpoint is the quantification of the effect of the clinical<br /><br>introduction of transcutaneous carbon dioxide monitoring during laryngoscopic<br /><br>and microlaryngeal procedures in children. Therefore, the main study parameter<br /><br>is the cumulative carbon dioxide load / shortage, as a fraction of the<br /><br>monitoring time and will be compared between the *pre* and *post* timeframes. </p><br>
Secondary Outcome Measures
NameTimeMethod
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