Comparative study of fibroptic bronchoscopic with two method: midazolam base versus lidocaine base
Not Applicable
Recruiting
- Conditions
- bronchoscopy.
- Registration Number
- IRCT20110103005536N8
- Lead Sponsor
- Artesh University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 140
Inclusion Criteria
male and female patients aged 18 to 80 years
ASA I-II
Exclusion Criteria
People with a history of sore throat and lung disease with 90% o2sat (hypoxemia)
People with Ejection fraction less than 40%
people with hearth rate less than 50
people with hypotension less than 90 mmHg
People with III and grade II conduction blocks
People with liver failure (2-fold increase in liver enzymes) and kidney failure (creatinine more than 2 mg / dL)
Pregnant or lactating women
People With a history of long-term use of antipsychotic drugs or sedatives.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Type of basic anesthetic. Timepoint: Before the intervention. Method of measurement: Based on the name of the drug.
- Secondary Outcome Measures
Name Time Method Complications of bronchoscopy. Timepoint: During the intervention. Method of measurement: Based on the need for intubation, nausea, decreased oxygen saturation, sore throat, cough.;Duration of bronchoscopy. Timepoint: During the intervention. Method of measurement: Based on time from start to end of the procedure.;Physician satisfaction. Timepoint: After the intervention. Method of measurement: Based on the doctor's satisfaction with the procedure from 1 to 5 based on likret scale.;Patient satisfaction. Timepoint: After the intervention. Method of measurement: Based on the patient's satisfaction with the procedure from 1 to 5 based on likret scale.