Surgery with general anesthesia.
Conditions
Interventions
Intervention 1: Control group: In this group, patients will receive 2 cc of normal saline before anesthesia. Intervention 2: First intervention group: In this group, patients will receive 0.15 mg/kg o
Sponsors
Esfahan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: Age range 18 to 60 years With ASA I or II Candidate for general surgery with local anesthesia
Exclusion criteria
Exclusion criteria: BMI less than 18 or more than 31 kg/m2 History of heart failure, heart block Liver or kidney disease Dementia History of allergy to any of the drugs used Pregnancy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: Following the injection of etomidate until the patient is completely anesthetized. Method of measurement: Score 0 (no pain) to 10 (most severe pain).;Myoclonic movements. Timepoint: Following the injection of Etomidate. Method of measurement: Score 0 to 3 (Score 0: no myoclonus, score 1: mild myoclonus (in the wrist only), score 2: moderate myoclonus (in the arm, elbow or shoulder), and score 3: severe myoclonus (generalized response or in more than one limb, apnea, nausea, vomiting and itching)).;Heart rate. Timepoint: Before the injection of Etomidate, immediately after full anesthesia. Method of measurement: Monitoring device.;Mean arterial pressure. Timepoint: Before the injection of Etomidate, immediately after full anesthesia. Method of measurement: Monitoring device. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactBehzad Nazemroaya
Esfahan University of Medical Sciences
Outcome results
None listed