To compare effect of prophylactic lignocaine and dexamethasone nebulisation on sore throat after endotracheal intubation.
Not Applicable
- Conditions
- Health Condition 1: J069- Acute upper respiratory infection,unspecified
- Registration Number
- CTRI/2020/11/029013
- Lead Sponsor
- GGSMCH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1) Adult patients with equal numbers of males and females aged between 20 and 55 years.
2) Patients belonging to ASA I or II.
Exclusion Criteria
1) Refusal of patient to give consent.
2) Known allergic to lignocaine or dexamethasone.
3) Patients belonging to ASA III or IV.
3) Anticipated difficult intubation.
4) Patients requiring >2 attempts at intubation or requiring bougie for intubation.
5) Patients on corticosteroids or any other anti inflammatory analgesic.
6) Patients undergoing head and neck surgeries.
7) Patients having renal, hepatic dysfunction or cardiovascular dysfunction.
8) Psychiatric disorders or drug abuse.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the effect of prophylactic nebulisation with lignocaine and dexamethasone on incidence and severity of post operative sore throat after endotracheal intubation. <br/ ><br>Timepoint: Post operatively at 0, 6, 12, 24 hour <br/ ><br>
- Secondary Outcome Measures
Name Time Method To compare the effect of prophylactic nebulisation with lignocaine and dexamethasone on incidence and severity of post operative cough and hoarseness of voice after endotracheal intubation. <br/ ><br>Timepoint: Post operatively at 0, 6, 12, 24 hour