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High Flow Nasal Cannula versus Low Flow Nasal Cannula in patienst with atrial fibrillation undergoing point-by-point catheter ablation under deep sedation.

Recruiting
Conditions
Oxygenatie tijdens diepe sedatie
desaturation
Hypoxemia
10007521
10007593
Registration Number
NL-OMON52794
Lead Sponsor
Medisch Universitair Ziekenhuis Maastricht
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
210
Inclusion Criteria

Adults undergoing elective RFCA or Galaxy PFAfor atrial fibrillation in the
Maastricht UMC Cardiac Catheter Labs under deep sedation administrated by a
clinician anesthesiology.

Exclusion Criteria

Age under 18 years
Body Mass Index > 32
Diagnosed sleep apnoea syndrome
Chronic pulmonary obstructive disease gold IV and COPD gold III with recent or
frequent exacerbation
Diagnosed pulmonary or cardiac condition requiring chronic oxygen therapy
Complete nasale obstruction
Active nose bleeding
Untreated pneumothorax (pre- existing)
Recent upper airway surgery
Recent base of skull fracture
Expected difficult airway.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>Lowest saturation is the measured and main outcome. </p><br>
Secondary Outcome Measures
NameTimeMethod
<p>Secondary objectives of the study are the duration of the lowest SpO2,<br /><br>incidence of cross over, incidence of desaturation, adverse sedation events,<br /><br>peak transcutaneous carbon dioxide (TcCO2), mean TcCO2, satisfaction of<br /><br>patients with sedation, patients comfort with oxygen delivery, rating of<br /><br>clinician of the anaesthesiology department of difficulty maintaining<br /><br>oxygenation status, rating of clinician anaesthesiology of user-friendliness of<br /><br>the oxygen delivery device and satisfaction of cardiologists with catheter<br /><br>stability in relation to sedation. </p><br>
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