Sore throat after endotracheal intubation. Anaesthesiology devices associated with adverse incidents
Conditions
Interventions
Intervention 1: Intervention group: In the Lidocaine group, the endotracheal tube cuff will be filled with lidocaine 2% until the pressure reaches between 20 and 25 cm H2O. Intervention 2: Control gro
Sponsors
Qazvin University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
20 Years to 60 Years
Inclusion criteria
Inclusion criteria: Female Gender Age between 20 to 60 Class 1 & 2 of the American Society of Anesthesiologists (ASA) Classification
Exclusion criteria
Exclusion criteria: Heart block Heart Failure Unstable hemodynamics Depression Kidney or liver failure Sensitivity to Lidocaine Tracheal deformity Lack of consent to participate in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Blood pressure. Timepoint: Before induction of anesthesia, 30 and 60 minutes after induction, and before and after extubation. Method of measurement: Blood Pressure Cuff (Sphygmomanometer).;Heart rate. Timepoint: Before induction of anesthesia, 30 and 60 minutes after induction, and before and after extubation. Method of measurement: Cardiac monitoring device. | — |
Secondary
| Measure | Time frame |
|---|---|
| Coughing. Timepoint: During recovery, 6 hours and 12 hours after recovery. Method of measurement: Patient self-reporting.;Bucking. Timepoint: During recovery, 6 hours and 12 hours after recovery. Method of measurement: Patient self-reporting.;Sore throat. Timepoint: During recovery, 6 hours and 12 hours after recovery. Method of measurement: Patient self-reporting. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactKaran Samimi
Qazvin University of Medical Sciences
Outcome results
None listed