Overview

The Effects of Lidocaine and Magnesium Sulphate on the Attenuation of the Hemodynamic Response to Tracheal Intubation

Status:
Completed
Trial end date:
2014-11-01
Target enrollment:
0
Participant gender:
All
Summary
Justification and Objectives: The hemodynamic response to stimuli of the airways is a common phenomenon and its control is important to decrease systemic repercussions. The objective of this study is to compare the effects of intravenous administration of Magnesium Sulphate versus Lidocaine in the hemodynamics of this reflex after laryngoscopy and tracheal intubation. Methods: This double blind, randomized, single center, and prospective study evaluated 56 patients, ASA 1 or 2, aged between 18 and 65 years, scheduled for elective surgeries under general anesthesia with tracheal intubation. Patients were divided into two groups. Group M received 30mg/kg of Magnesium Sulphate, and group L 2 mg/kg of Lidocaine through continuous infusion, immediately before induction of anesthesia. The values for blood pressure (BP), heart rate (HR) and bispectral index (BIS) were measured in both groups at six distinct moments related to the administration of the drugs under study.
Phase:
Phase 4
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Hospital de Base
Treatments:
Anesthetics
Lidocaine
Magnesium Sulfate
Criteria
Inclusion Criteria:

- ASA 1 or 2, aged between 18 and 65 years, scheduled for elective surgeries with
orotracheal intubation at the Hospital de Base do Distrito Federal, Brazil

Exclusion Criteria:

- Patients who have contraindication or a history of hypersensitivity to the drugs
involved in the work

- Patients with ischemic heart disease, atrioventricular block in any degree, diagnosed
cardiac arrhythmias, heart failure

- Renal failure carrier

- Users of beta-blockers or calcium channel blockers,

- Patients who have forecast of difficult tracheal intubation,

- BMI < 35 kg/m2,

- Patients in whom neuroaxis block was performed before the induction of anesthesia,

- Patients who refused to participate in the study

- Those who needed two or more laryngoscopy attempts to position the orotracheal tube,

- Any other condition that, in the researchers' opinion, could offer risks to the
patient