Succinylcholine Adverse Effects. Skeletal Muscle Relaxants [Neuromuscular blocking agents]
Conditions
Interventions
Intervention 1: Placebo First Group: Normal saline, IV injection, Before induction of Anesthesia. Intervention 2: Atracurium Third Group: 0.03 mg/kg, IV injection, Before induction of Anesthesia. Int
Placebo
Treatment - Drugs
Placebo First Group: Normal saline, IV injection, Before induction of Anesthesia
Atracurium Third Group: 0.03 mg/kg, IV injection, Before induction of Anesthesia
Succinylcholine Second Group: 5 mg, IV injection, Before induction of Anesthesia
Sponsors
Shiraz University of Medical Science
Eligibility
Sex/Gender
All
Age
76 Years to 44 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria:ASA Iand II,Age between 18-50 years old.Exclusion criteria:Patients with severe trauma in the last 24-48 hours,Burns,Muscular dystrophy,Malignant hyperthermia, Patients that ICP and IOP are harmful for them.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Potassium level after intravenous injection of succinylcholine drug. Timepoint: Before surgery, 8 hours after surgery, 16 hours after surgery. Method of measurement: Concentration in blood mEq/l.;Pain level after intravenous injection of succinylcholine drug. Timepoint: Day after surgery. Method of measurement: Fill questionnaire and Asking patient aboat pain and Visual Scale.;Fasciculation level after intravenous injection of succinylcholine drug. Timepoint: After injection of drug. Method of measurement: Fill questionnaire and Visual Scale.;Potassium level after Intravenous injection of atracurium. Timepoint: Before surgery?8hours after surgery?16hours after surgery. Method of measurement: Concentration in blood mEq/l.;Pain level after intravenous injection of atracurium drug. Timepoint: Day after surgery. Method of measurement: Fill questionnaire and Asking patient about pain and visual scale.;Fasciculation level after intravenous injection of atracurium drug. Timepoint: After injection of drug. Method of measurement: Fill questionnaire and visual scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. Hamidreza Bahmani
Shiraz University of Medical Sciences
Outcome results
None listed