The effect of using three anesthesia methods with propofol, sevoflurane, and dexmedetomidine on respiratory complications in children aged 1 month to 3 years undergoing fiber optic bronchoscopy.
Phase 2
- Conditions
- Fiber optic bronchoscopy.
- Registration Number
- IRCT20200825048515N69
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 120
Inclusion Criteria
Children from 1 month to 3 years
Candidate for diagnostic fiber optic bronchoscopy
ASA equal to I or II
Consent to participate in the study
Exclusion Criteria
Having comorbidity (Such as heart disease, metabolic disease, history of seizures, high ICP, porphyria, thyroid disease)
Therapeutic bronchoscopy (presence of foreign body, etc.)
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Blood pressure. Timepoint: upon entering the operating room, and every 5 minutes during bronchoscopy and every 15 minutes during recovery until the end of recovery. Method of measurement: Monitoring device.;Heart beat. Timepoint: upon entering the operating room, and every 5 minutes during bronchoscopy and every 15 minutes during recovery until the end of recovery. Method of measurement: Monitoring device.;Oxygen saturation (SpO2). Timepoint: upon entering the operating room, and every 5 minutes during bronchoscopy and every 15 minutes during recovery until the end of recovery. Method of measurement: Monitoring device.;Respiratory complications. Timepoint: During bronchoscopy. Method of measurement: Observation.
- Secondary Outcome Measures
Name Time Method