Elective general anesthesia. Diagnostic and monitoring anesthesiology devices associated with adverse incidents
Conditions
Interventions
Intervention 1: Intervention group: Use of a bispectral index (BIS). Intervention 2: Control group: Without Use of a bispectral index (BIS).
Sponsors
Zahedan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1- ASA Class I & II population between the ages of 18 and 65
Exclusion criteria
Exclusion criteria: -History of intubation problem before or in doubt Loss of consciousness before surgery without reason Brain surgery Cardiovascular disease Esophageal reflax6- Hiatus hernia liver or renal failure sensitivity to the drugs Sedative or substance administration within 24 hours before surgery History of any neurological disorders and use of psychiatric drugs Patient history of addiction1 hemoglobin < 10 mg/dL Patient dissatisfaction with study participation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Amount of propofol. Timepoint: 20 seconds. Method of measurement: Syringe.;Mean arterial pressure. Timepoint: before induction (baseline), immediate after induction, immediate after intubation, and 5 min after intubation. Method of measurement: Sphygmomanometer.;Heart beat. Timepoint: before induction (baseline), immediate after induction, immediate after intubation, and 5 min after intubation. Method of measurement: heart rate monitor. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMaryam Hojjat
Zahedan University of Medical Sciences
Outcome results
None listed