prevention of sore throat after tracheal intubation. Anaesthesiology devices associated with adverse incidents
Conditions
Interventions
Intervention 1: First group: Intracuff application of 16 mg dexamethasone. Intervention 2: Third group: application of bethametasone ointment on endotracheal tube cuff. Intervention 3: Second group: I
Prevention
First group: Intracuff application of 16 mg dexamethasone.
Third group: application of bethametasone ointment on endotracheal tube cuff.
Second group: Intravenous application of 8 mg dexamethasone.
Fourth group or control group: filling the endotracheal tube cuff with air.
Sponsors
Ladan Ansari
Islamic Azad University, Tehran Medical Branch, Vice chansellor for research
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: 60>age>18 yr; ASA class 1 or 2; no URI infection or sorethroat at the time of surgery; no possibility of difficult air way; no candidate of surgery on air way; candidate of general anesthesia & tracheal intubation; no contraindication for receiving steroids. Exclusion criteria: intraoperation pharyngeal packing; intraoperation NG tube placement.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sore throat after tracheal intubation. Timepoint: After recovery period, 8 & 24 hours after intervention. Method of measurement: Questionaire & VAS method. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactLadan Ansari
Tehran Medical Branch of Islamic Azad University
Outcome results
None listed