Effect of filling of endotracheal tube cuff with Lidocaine on complications of postoperative extubatio
Not Applicable
Completed
- Conditions
- Sore throat after endotracheal intubation.Anaesthesiology devices associated with adverse incidents
- Registration Number
- IRCT20150803023473N5
- Lead Sponsor
- Qazvin University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 70
Inclusion Criteria
Female Gender
Age between 20 to 60
Class 1 & 2 of the American Society of Anesthesiologists (ASA) Classification
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
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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 Outcome Measures
Name Time Method 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.