Effect of Propofol on vital signs and assessing the level of anesthesia
Not Applicable
- Conditions
- anesthesia.Dissociative anaesthesia and sensory loss
- Registration Number
- IRCT2015030218099N3
- Lead Sponsor
- Vice chancellor for research, Shahrekord University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 92
Inclusion Criteria
Aged between 20 and 80 years old, patients under surgery with general Anesthesia, patients with class I and ASA class II.
Exclusion criteria: any observable unpredictable complications after injection of propofol; patients with ASA class higher than I and II, patients with drug sensitivity, and patients with contraindications due to the use of this drug.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Movement Score. Timepoint: 1 min after the induction of anesthesia. Method of measurement: observation.;Blood pressure. Timepoint: 5 min before induction of anesthesia,1 min and 5min after induction of anesthesia and after intubation. Method of measurement: monitoring devices.;Level of consciousness. Timepoint: 5 minutes before induction of anesthesia, 1 minute and 5 minutes after intervention and after intubation. Method of measurement: BIS monitoring set.
- Secondary Outcome Measures
Name Time Method