Diagnostic biopsy under direct laryngoscopy.
Conditions
Interventions
Intervention 1: Intervention group 1: succinylcholine.The first group will receive 3 micrograms / kg of fentanyl and 0.5 mg / kg of lidocaine for premedication, and will be induced with 1 mg / kg of s
Sponsors
Iran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
20 Years to 50 Years
Inclusion criteria
Inclusion criteria: Patients 20 to 50 years without a history of disease or with a controlled disease
Exclusion criteria
Exclusion criteria: The patients with a history of psychiatric illness The patients with a history of peritonitis The patients with a history of hyperkalemia The patients with a history of renal and hepatic failure The patients with a history of malignant hyperthermia and pseudocholinesterase deficiency The patients with a history of addiction The patients with a history of benzodiazepines The patients with a history of burns
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Agitation. Timepoint: From the moment of closing the gas until 10 minutes after estubation for once. Method of measurement: Emergency agitation of patients from the moment of gas closure until 10 minutes after extubation will be performed according to the criteria of Ricker Sedation Agitation Scale.;Myalgia. Timepoint: Myalgia pain scores will be recorded 1, 4, 8 and 24 hours after surgery. Method of measurement: Examination by a Physician. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr Saeid Amniati
Iran University of Medical Sciences
Outcome results
None listed