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A scientific experiment to study the attenuation of intubation response with dexmeditomedine nebulization & sublingual nitroglycerin spray

Not Applicable
Conditions
Health Condition 1: O- Medical and Surgical
Registration Number
CTRI/2023/12/060709
Lead Sponsor
Department of Anesthesiology
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

Age group 18 - 60 years

Both genders

ASA grade I and II

Exclusion Criteria

Patient refusal

Pregnancy

Emergency surgery

Patient with anticipated difficult airway

Modified mallampatti III and IV

Laryngoscope and intubation time >20s

Obese patients with BMI >30kg/m2

H/o chronic hepatic renal or cardiac disease

H/o drug allergy

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Attenuation of intubation response with dexmeditomedine nebulization versus sublingual nitroglycerin sprayTimepoint: Baseline <br/ ><br>At induction <br/ ><br>1 min after induction <br/ ><br>2 min after induction <br/ ><br>3 min after induction <br/ ><br>At intubation <br/ ><br>1 min after intubation <br/ ><br>2 min after intubation <br/ ><br>3 min after intubation <br/ ><br>5 min after intubation <br/ ><br>10 min after intubation <br/ ><br>15 min after intubation <br/ ><br>30 min after intubation <br/ ><br>At extubation <br/ ><br>5 min after extubation <br/ ><br>10 min after extubation <br/ ><br>15 min after extubation <br/ ><br>20 min after extubation <br/ ><br>25 min after extubation <br/ ><br>30 min after extubation
Secondary Outcome Measures
NameTimeMethod
Adverse effects of dexmeditomedine and nitroglycerinTimepoint: 24 hours
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