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Effect of Dexmedetomidine Premedication on Attenuation of Stress Response to Laryngoscopy and Endotracheal Intubatio

Phase 4
Recruiting
Conditions
Anaesthesia
Registration Number
PACTR202402608586239
Lead Sponsor
natioanl liver institute
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
84
Inclusion Criteria

(1)Adult patients who will have elective surgical operations under general anesthesia.
(2)Age: Patients age 18–65 years, of both sexes.
(3)American Society of Anesthesiologists (ASA) grade I–II
(4)Body mass index (BMI) 18.5–35 kg/m2.
(5)Airway of Modified Mallampati Grade I and II

Exclusion Criteria

(1)Patient refusal to participate in the study.
(2)Morbid obesity Body mass index higher than 35 kg/m2
(3)Patients with pacemakers and cardiac arrhythmia.
(4)Uncontrolled diabetes mellitus, hypertension, ischemic heart disease, , history of myocardial, pulmonary, or endocrine diseases, , hepatic or renal impairment.
(5)Pregnancy, full stomach, emergency surgery.
(6)Patients who are allergic to any of the study drugs, those with opioid addiction.
(7)Patients on beta blocker or calcium channel blocker.
(8)Patients who had Cormack Lahane score III and above and also those in which the duration of laryngoscopy lasted more than 25 seconds.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
compare changes in analgesia nociception index [ANI] during direct laryngoscopy and endotracheal intubation in patients undergoing elective surgeries after premedication by dexmedetomidine in two different doses
Secondary Outcome Measures
NameTimeMethod
to find out the optimum dose of dexmedetomidine given as premedication according to changes in the ANI correlated to hemodynamics
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