An observation study to study the efficiency and reduction in incidence of sore throat hoarsness of voice and cough when two different lubricating agents are use for proper placement of the airway device .
Not Applicable
Completed
- Conditions
- Health Condition 1: null- ASA GRADE 1 AND 2Health Condition 2: C00-D49- Neoplasms
- Registration Number
- CTRI/2017/10/010058
- Lead Sponsor
- VENUGOPAL A
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 118
Inclusion Criteria
1)All American society of Anaesthesiologists (ASA)
Grade I and II patients
2)Surgery under general Anaesthesia with controlled ventilation
3)Age of 18 and 60 years
Exclusion Criteria
1)Recent or on going history of sore throat
respiratory tract infection
2)On going steroid therapy
3)Congenital facial abnormalities
4)Nasogastric tube in situ
5)Restricted mouth opening ( <3 cm).
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Incidence of sore throat, <br/ ><br>hoarseness of voice and cough on administration as lubricating agentTimepoint: 2,6,12,24th Hour postoperative period
- Secondary Outcome Measures
Name Time Method Trauma and oral cavity bleeds due to placementTimepoint: 2,6,12,24th Hour post operative period