Complication of intubation. Failed or difficult intubation
Conditions
Interventions
Intervention 1: The observer will fill endotracheal cuff randomly with normal saline in group N. Intervention 2: The observer will fill endotracheal cuff randomly with Lidocaine in group L. Interventi
Behavior
Prevention
The observer will fill endotracheal cuff randomly with normal saline in group N.
The observer will fill endotracheal cuff randomly with Lidocaine in group L.
The observer will fill endotracheal cuff randomly with Dexamethasone in group D.
Sponsors
Research Assistance of AJA University of Medical Science
Eligibility
Sex/Gender
Male
Age
20 Years to 50 Years
Inclusion criteria
Inclusion criteria: The inclusion criteria for this study are being: male sex, non-smoker, not suffering from any disease related to air ways like asthma, bronchitis and amphysma, not having cold during last 6 weaks, not using corticosteroids and analgesics before operation. Our exclusion criteria are factors predictive of difficult intubation (number of tracheal intubation attempts), and the need for a nasogastric tube Patients with any preoperative sore throat or hoarseness or any airway condition resulting in an ASA physical status greater than II3,12.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Cough. Timepoint: Every 6 hours. Method of measurement: History taking and physical examination.;Sore throat. Timepoint: Every 6 hours. Method of measurement: History taking and physical examination.;Laryngospasm. Timepoint: Every 6 hours. Method of measurement: Physical examination. | — |
Secondary
| Measure | Time frame |
|---|---|
| Weight. Timepoint: Before start of intervention. Method of measurement: weigh.;Age. Timepoint: Before start of intervention. Method of measurement: Patient identification card. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr Mohamad Reaz Rafiei
AJA University of Medical Science
Outcome results
None listed