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Preoperative pharmacological intervention for prevention of post operative sore throat and hoarseness.

Not Applicable
Conditions
Health Condition 1: R69- Illness, unspecified
Registration Number
CTRI/2019/02/017804
Lead Sponsor
ilavati Hospital and Research Centre
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1) Age 18-75 yrs

2) Male and female patients undergoing elective surgery under general anaesthesia in supine position needing endotracheal intubation

3) American Society of Anesthesiologists (ASA) physical status I-II patients

4) Duration of surgery between 60 mins and 300 mins

5) Mallampatti classification I & II

Exclusion Criteria

1)Recent history of respiratory tract infection or preoperative sore throat

2)More than one attempt at tracheal intubation

3)Pregnant and lactating females

4)Head and neck surgeries

5)Chronic steroid or NSAID(non steroidal anti inflammatory drugs) therapy

6)Known asthmatic or chronic obstructive pulmonary disease

7)Vulnerable subjects

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Comparison of preoperative nebulised ketamine and intravenous dexamethasone used alone or in combination for the prevention of postoperative sore throat and hoarseness.Timepoint: To compare the incidence and severity of post perative sore throat and hoarseness graded on a four point scale at immediate recovery, 3hrs, 6hrs, 12hrs and 24hrs post operatively <br/ ><br> <br/ ><br>
Secondary Outcome Measures
NameTimeMethod
To study the incidence of adverse effects such as nausea, vomiting. <br/ ><br> <br/ ><br>Timepoint: Occurance of nausea and vomiting at immediate recovery, 3hrs, 6hrs, 12hrs and 24hrs post operatively . <br/ ><br>
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