Controlled comparison between lidocaine and beclomethasone spray to reduce postoperative sore throat and cough
Phase 2
- Conditions
- Complication of intubation.Anaesthesiology devices associated with adverse incidents
- Registration Number
- IRCT201012135381N1
- Lead Sponsor
- Vice-chancellor of Research Babol University Of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 90
Inclusion Criteria
ASA physical status I to II; aged 18 to50years; surgical procedures under general anesthesia with orotracheal intubation in the supine position; not using corticosteroids and analgesics before operation.
exclusion criteria: patients undergoing oral cavity surgery; cervical spine surgery; thyroid surgery;patients with a difficult airway (after >1 orotracheal intubation attempt); smoker; history of bronchial asthma; requiring a nasogastric tube;or a history of perioperative sore throat.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Sore throat. Timepoint: 1 and 24 hour after extubation. Method of measurement: history taking.;Cough. Timepoint: 1 and 24 hour after extubation. Method of measurement: history taking.;Hoarseness. Timepoint: 1 and 24 hour after extubation. Method of measurement: history taking.
- Secondary Outcome Measures
Name Time Method Blood pressure. Timepoint: Before intubation, 1,3,5 minutes after intubation, before extubation, 1,3,5 minutes after intubation. Method of measurement: Noninvasive cuff measurrment.;Heart rate. Timepoint: Before intubation, 1,3,5 min after intubation,, before extubation, 1,3,5minutes after intuba minutes after intubation. Method of measurement: Pulse counting.