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Effect of duration of procedural sedation on postprocedural respiratio

Recruiting
Conditions
Atelectasis, upper respiratory tract infections
Registration Number
NL-OMON21394
Lead Sponsor
MCG
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
100
Inclusion Criteria

oPlanned for procedure under PSA performed by the department of anesthesiology
oPassed screening for PSA
oProcedure will potentially last longer than 2 hours
oProcedure performed in prone position
oSpO2 on room air pre-procedurally > 96%

Exclusion Criteria

oProcedure with prolonged esophageal or bronchial manipulation
oASA status IV
oCOPD Gold 3-4
oprevious lung surgery
ouse of CPAP for OSAS
oUse of FiO2 > 50% during procedure
oUse of endotracheal intubation during procedure
oUse of Optiflow during procedure
oneed for additional bolusses of esketamine during the procedure

Study & Design

Study Type
Observational non invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Atelectasis after procedural sedartion
Secondary Outcome Measures
NameTimeMethod
Signs and symptoms of upper respiratory tract infections
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