Survey of anesthesia for direct laryngoscopy..
Conditions
Interventions
Intervention 1: Intervention group 1: After induction of anesthesia,patients in group Awill be received an IV infusion of dexmedetomidine 1 mcg/Kg over five minutes with a 20 ml syringe with the label
Sponsors
Shiraz University of Medical Sciences
Eligibility
Sex/Gender
All
Age
20 Years to 70 Years
Inclusion criteria
Inclusion criteria: All patients who will candidate for direct laparoscopy under general anesthesia will be enrolled.
Exclusion criteria
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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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
| Measure | Time frame |
|---|---|
| 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. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMohammadAli Sahmeddini
Shiraz University of Medical Sciences
Outcome results
None listed