Sedation in bronchoscopy
Phase 1
Recruiting
- Conditions
- Sedation for bronchoscopy.
- Registration Number
- IRCT20130304012695N18
- Lead Sponsor
- Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 70
Inclusion Criteria
All candidates for fiberoptic bronchoscopy aged 20-70 years who need sedation
Exclusion Criteria
Patients who have a history of drug addiction or are taking methadone
Patients who take neurologic or psychoactive drugs
Patients with a history of renal and liver failure
History of allergy to diphenhydramine
History of ischemic heart disease
Patients with hemodynamic instability
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The degree of sedation and agitation. Timepoint: At the beginning and 2, 5, 10 and 15 minutes of bronchoscopy. Method of measurement: Based on the criteria of the Richmond Agitation Sedation Scale.;Amount of propofol boluses in cases of insufficient sedation. Timepoint: Agitation degree greater than one during bronchoscopy. Method of measurement: At the end of bronchoscopy based on mg.;Hemodynamic indicators ,heart rate and blood pressure. Timepoint: Before drug induction and 5, 10 and 15 minutes after starting bronchoscopy and during recovery. Method of measurement: From patient monitoring.;Hypoxemia. Timepoint: During bronchoscopy. Method of measurement: By pulse oximetry.;Recovery time. Timepoint: From the end of bronchoscopy to the time of leaving the bronchoscopy department. Method of measurement: By the Chronometer based on minutes.
- Secondary Outcome Measures
Name Time Method