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Bolus administration versus continuous infusion of Propofol sedation in flexible bronchoscopy

Completed
Conditions
Pulmonary disease diagnosis, need for flexible bronchoscopy
Respiratory
pulmonary disease, need for flexible bronchoscopy
Registration Number
ISRCTN66129676
Lead Sponsor
niversity Hospital Basel (Switzerland)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
702
Inclusion Criteria

1. Patients aged 18 or older
2. Patients undergoing flexible bronchoscopy

Exclusion Criteria

1. Known allergy to propofol
2. Mental disorder preventing appropriate judgment concerning study participation
3. Pregnancy and breast-feeding
4. Intubated patients

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1. Number (percentage) of complications (oxygen desaturation less than or equal to 90%<br>2. Need for chin-support<br>3. Need for nasopharyngeal or oropharyngeal airway insertion<br>4. Need for intubation<br>5. Hypotension with a systolic blood pressure of less than 90 mmHg<br>6. Minor or major bleeding<br>7. Intensive Care Unit [ICU] need post-bronchoscopy<br>8. Pneumothorax<br>9. Need to abort bronchoscopy<br>10. Death<br>These outcomes are assessed by the study physician during and up to 24 hours after the procedure
Secondary Outcome Measures
NameTimeMethod
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