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Comparison of conventional laryngoscope with video laryngoscope.

Not Applicable
Conditions
Health Condition 1: null- Those requiring surgery
Registration Number
CTRI/2018/05/014150
Lead Sponsor
Gurleen Kaur
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1. 120 patients of either sex

2. Age 20-70

3. ASA grade 1 and II

4. MPG I, II, III and IV

Exclusion Criteria

1. Patient refusal

2. Age < 20 and > 70 years

3. ASA III and IV

4. Patients with pulmonary aspiration of gastric contents ( e.g. pregnancy, diabetes )

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1. Duration of laryngoscopy and intubation <br/ ><br>2. Cormack â?? Lehane grading. <br/ ><br>3. Evaluate ease of intubation.Timepoint: 0-10 minutes after intubation
Secondary Outcome Measures
NameTimeMethod
1. Number of attempts and any optimisation manoeuvres required for intubation. <br/ ><br>2. Hemodynamic response. <br/ ><br>3. Any trauma caused due to laryngoscopy.Timepoint: During same time frame
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