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A STUDY BETWEEN TWO DRUGS WHICH DECREASE THE RESPIRATORY SIDE EFFECTS POST GENERAL ANAESTHESIA.

Phase 3
Conditions
Health Condition 1: O- Medical and Surgical
Registration Number
CTRI/2021/05/033489
Lead Sponsor
Bharati Hospital and Research Center
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1) Patients with ASA I,II,III GRADE

2) Patients with schedule of surgery for more than 2 hours

Exclusion Criteria

1. Undergoing surgeries of oral cavity and pharynx with anticipated difficult airway.

2. Use of nasogastric tube and throat packs.

3. History of smoking, history of Bronchial Asthma and COPD.

4. Using corticosteroids before surgery.

5. Intubation attempts more than once.

6. Patient refusal in participation in the study.

7. Hypersensitivity to local anaesthetics.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
SORE THROATTimepoint: 24 hours
Secondary Outcome Measures
NameTimeMethod
COUGH,HOARSENESSTimepoint: 24 hours
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