Comparison of quality anesthesia of two anesthetic drugs in direct laryngoscopy.
Phase 3
Recruiting
- Conditions
- Survey of anesthesia for direct laryngoscopy..
- Registration Number
- IRCT20121204011662N13
- Lead Sponsor
- Shiraz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
All patients who will candidate for direct laparoscopy under general anesthesia will be enrolled.
Exclusion Criteria
Patients with history of ischemic heart disease
Patients with history of heart failure
Patients with history of asthma
Patients with history of renal failure
Patients with history of hepatic failure
Patients who are morbidly obese
Patients in emergency situation
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Mean arterial blood pressure (MAP). Timepoint: Values will record at baseline, 5, 10, 15, 30, and 45, minutes. Method of measurement: Non invasive blood pressure monitoring.;Heart rate per minute. Timepoint: Values will record at baseline, 5, 10, 15, 30, and 45, minutes. Method of measurement: Electrocardiogram.
- Secondary Outcome Measures
Name Time Method Sedation Score. Timepoint: Every 15 minutes in recovery room. Method of measurement: Ramsay Scale.;Attacks of respiratory depression. Timepoint: Every 15 minutes in recovery room. Method of measurement: Defined as a respiratory rate < 8 breaths/min.;Incidence of nausea and vomiting. Timepoint: Every 15 minutes in recovery room. Method of measurement: 0: No nausea and vomiting, 1: Nuasea without Vomiting, 2: Both Nausea and Vomiting.;Severity of postoperative pain. Timepoint: Every 15 minutes in recovery room. Method of measurement: Visual analogue Scale.