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comparing the effectiveness of nebulization by 2 drugs in reducing sore throat after surgery

Not Applicable
Conditions
Health Condition 1: O- Medical and Surgical
Registration Number
CTRI/2023/03/050439
Lead Sponsor
DR KIRAN A V
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1.Patients belonging to American Society of Anaesthesiologists Physical Status grade I and II.

2.Patients posted for elective surgeries under general anaesthesia with tracheal intubation less than 4 hours.

3.Patients between age group 18 to 60 years.

4.Patients willing to give informed consent to participate in the study.

5.Mallampatti grade I and II.

6.Laryngoscopy done by experienced anaesthesiologist in single attempt.

Exclusion Criteria

1.Patients with known hypersensitivity or contra-indications to study drugs.

2.Received drugs(other than study drugs) that prevent sore throat, 24 hours before anaesthesia..

3.Patients with Body mass index more than 30.

4.ASA grade III and IV

5.Mallampatti III and IV

6.History of URTI in previous 2 weeks

7.H/O smoking

8.More than 2 attempts at laryngoscopy and intubation

9.Patients who are on steroids

10.Patients requiring manipulation of airway or instrumentation(like oral airway,stylet,bougie, external laryngeal maneuver)

11.Pregnant patients

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To compare the efficacy of dexamethasone nebulization versus lignocaine nebulization in prevention or reduction of post operative sore throat(POST)Timepoint: 0 hour , 2 hours , 4 hours , 6 hours , 12 hours , 24 hours
Secondary Outcome Measures
NameTimeMethod
To compare the efficacy of dexamethasone nebulization versus lignocaine nebulization in prevention or reduction of post operative hoarseness and cough.Timepoint: 0 hours , 2 hours , 4 hours , 6 hours , 12 hours , 24 hours
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