Evaluation of anesthesia quality with three methods: propofol + fentanyl Vs propofol + fentanyl + lidocaine Vs propofol + fentanyl + lidocaine + ketamine in patients referred to the scoping ward
Phase 3
- Conditions
- .
- Registration Number
- IRCT20200921048789N2
- Lead Sponsor
- Artesh University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
All patients who are candidates for scoping in 501 Army Hospital in 2021
Exclusion Criteria
Age under 18 and over 70 years
ASA classification 4 or 5
History of uncontrolled blood pressure
History of Chronic Obstructive Pulmonary Disease (COPD)
History of psychotic or neurological disorders
History of seizures
History of use of drugs affecting the central nervous system
Pregnancy
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Frequency of cough. Timepoint: During and after the intervention. Method of measurement: View on the patient bed.;Duration of recovery. Timepoint: After intervention. Method of measurement: View on the patient bed.
- Secondary Outcome Measures
Name Time Method O2 saturation. Timepoint: During and after the intervention. Method of measurement: view on the patient's bed.