Effects of Intravenous Lidocaine Associated With Magnesium Sulfate on the Cisatracurium-Induced Neuromuscular Block

December 10, 2015 updated by: Waynice N.P. Garcia, University of Sao Paulo

Effect of Intravenous Infusion of Magnesium Sulfate Associated or Not to Lidocaine On the Neuromuscular Blockade Induced by Muscle Relaxant Cistracurium

The magnesium sulfate and lidocaine have been increasingly used alone or in combination during anesthesia procedure to meet various objectives, such as reduction of pain, use of smaller anesthetic doses and stabilization of hemodynamic parameters.

These medicines are often used in combination with neuromuscular blocking agents, which may contribute to the occurrence of residual block in some patients after anesthetic procedures. It was estimated that only 1-3 % of patients with residual block developing clinically apparent events. In a small proportion of patients, the consequences of residual blockade are very serious and even lethal. It is estimated that 40 % of patients with muscle paralysis come to the post-anesthesia care unit (PACU).

Considering that: (a) magnesium sulfate and lidocaine are showing an increasing number of applications in various areas of medicine, (b) these medications stand out for their properties analgesic, anti-inflammatory, anti-arrhythmic, neuroprotective and capable of reducing the demand of anesthetics and opioids, (c) magnesium sulfate as lidocaine has been important part of the therapeutic arsenal to control a large number of diseases (d) the patient surgical surgery or potentially have benefited in particular from its effects, (and) these drugs have been used routinely in many medical services as well as adjuvants in anesthesia, (f) previous studies have shown that magnesium sulfate is able to prolong the duration of neuromuscular blockade by different types of muscle relaxants, with controversies about its effect on latency (g) the effect of lidocaine on the action of muscle relaxants in current literature have shown great controversy and (h) do not exist in the literature studies involving both drugs; the investigators aimed to investigate the effects of magnesium sulphate infused alone or associated with lidocaine on the neuromuscular blockade promoted by cisatracurium, as well as evaluate its possible hemodynamic repercussions. For this purpose the SM was infused in bolus, prior to tracheal intubation and continuously during the maintenance of general anesthesia; the Lidocaine, when associated and the Isotonic Solution were used in the same way and timeline as SM. As secondary objectives it has been proposed to evaluate if the Lidocaine with Magnesium Sulfate would be able to interfere with the hemodynamic stability of the patients in the study.

Study Overview

Detailed Description

The study was approved by the Medical Research Ethics Committee of the Hospital das Clinicas, of the Faculty of Medicine of Ribeirao Preto, University of Sao Paulo, Brazil; Its Unique Protocol ID is 5362/2013. This study was conducted with free written informed consent from the study subjects.

This report describes a prospective randomized clinical trial. The author states that the report includes every item in the checklist for a prospective randomized clinical trial.

The study was registered prior to patient enrollment. Forty-eight American Society of Anesthesiology patient classification status ASA I and II undergoing elective surgery were divided into three parallel groups. The M group received MS 40 mg.kg-1 as a bolus before the induction of anesthesia and 20mg.kg-1h-1 via continuous i.v. infusion during the operation period. The ML group received identical doses of MS combined with lidocaine 3 mg.kg-1 as a bolus before the induction of anesthesia and 3 mg.kg-1h-1 via continuous i.v. infusion during the operation period. The control group was administered a equivalent volume of isotonic solution. Anesthesia was maintained via propofol and remifentanil infusions. After loss of patient consciousness and administration of the bolus infusions, a 0.15 mg.kg-1 bolus of cisatracurium was administered to the patient over 5 s. No additional cisatracurium injections were performed. The patient's neuromuscular function was assessed every 15 s by measuring the adductor polis with a TOF Watch SX acceleromyograph. The primary endpoint was the time at which spontaneous recovery of a train-of-four (TOF) ratio of 90% as achieved. The systolic, diastolic and mean and heart rate were recorded and annotated at various times: M1- when the patient arrived in the operating room; M2- immediately before induction of anesthesia; M3- before the infusion of the tested solutions (saline, magnesium sulphate or magnesium sulphate associated with lidocaine); M4- five minutes after M3 (end of infusion loading dose of test solutions); M5 immediately before intubation; M6- one minute after tracheal intubation and M7 (a through f) - every fifteen minutes until the end of the study.

The sample size was calculated with a power of 80% to detect differences of 20% in the timing of clinical onset and the duration of the neuromuscular blockade (NMB). Quantitative variables were described as mean ± standard deviation. The normality of the distributions was tested for all variables in each group, using the non-parametric test of Shapiro-Wilk. When the variable normally distributed, we used the analysis of variance test (ANOVA) for comparison between groups. When differences were found between the groups, we used the Tukey test for multiple comparisons. When the variable is not normally distributed by applying the Shapiro-Wilk test, we used the Kruskal-Wallis test to compare the groups. When differences were found between the groups, we used the Dunn test for multiple comparisons. The critical level of significance was 5%.

During the analysis of the recovery characteristics of the neuromuscular blockade, all parameters based on the T1 response (DUR 25% DUR 75% and DUR 95%) were normalized considering the final T1 value when this response did not return to baseline (VIBY-MOGENSEN et al., 1996).

Study Type

Interventional

Enrollment (Actual)

48

Phase

  • Phase 4

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 60 years (ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Before the recruitment of patients, the study was approved by Brazil Platform (a national and unified basis of research involving human subjects records) and published by the ClinicalTrials.gov

Inclusion Criteria:

  • ASA I or II
  • BMI between 18 and 29

Exclusion Criteria:

  • Use of medications that could affect the neuromuscular blockade such as calcium channel inhibitors, anticonvulsants and lithium carbonate
  • Presence of neuromuscular, renal or hepatic dysfunction.
  • Hypermetabolic or hypometabolic states such as fever, infection, and hyperthyroidism or hypothyroidism
  • Acid-base disorder, congestive heart failure or conductive heart problems, and those who were being treated for cardiac arrhythmias

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: TRIPLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Group M

Magnesium Sulfate. In this group, the patients received magnesium sulfate 40 mg/Kg as a bolus and 20 mg/kg/h by continuous IV infusion during surgery.

After the bolus of magnesium sulfate, 0.15 mg/kg of cisatracurium was infused over 5 seconds.

Other Names:
  • Nimbex
Experimental: Group ML

Magnesium Sulfate plus Lidocaine. In this group, the patients received 40 mg/kg of Magnesium Sulfate plus 3 mg kg-1 lidocaine as a bolus and 20 mg/kg/h and 3 mg/kg/h, respectively, by infusion continuously during the surgery.

After the bolus of magnesium sulfate and lidocaine, 0.15 mg/kg of cisatracurium was infused over 5 seconds

Other Names:
  • Nimbex
Placebo Comparator: Group C

Isotonic Solution. In this group, the patients received the volume of isotonic solution equivalent to the volume of solution infused into experimental groups.

After the bolus of the isotonic solution , 0.15 mg/kg of cisatracurium was infused over 5 seconds

Other Names:
  • Nimbex

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Latency
Time Frame: Participants were followed during the anesthetic - surgical procedure, an average of 90 minutes

The latency is computed as the elapsed time to reduce the response of T1 to 5% of the initial contraction force after the infusion of cisatracurium.

This outcome meansure was presented in seconds.

Participants were followed during the anesthetic - surgical procedure, an average of 90 minutes
Clinical Duration
Time Frame: Participants were followed during the anesthetic - surgical procedure, an average of 90 minutes

The clinical duration is the elapsed time for T1 recovery = 25% (Dur25%) of the original value of T1 after the infusion of cisatracurium.

This outcome meansure was presented in minutes.

Participants were followed during the anesthetic - surgical procedure, an average of 90 minutes
Recovery Index
Time Frame: Participants were followed during the anesthetic - surgical procedure, an average of 90 minutes

The recovery index is the elapsed time between the T1 recovery =25% (Dur25%) and T1 =75% (Dur75%) after the infusion of cisatracurium.

This outcome meansure was presented in minutes.

Participants were followed during the anesthetic - surgical procedure, an average of 90 minutes
Final Recovery Index
Time Frame: Participants were followed during the anesthetic - surgical procedure, an average of 90 minutes

The final recovery index is the elapsed time between the T1 recovery = 25% (Dur25%) and T4 / T1 = 80% (TOF = 80%) after the infusion of cisatracurium.

This outcome measure was presented in minutes.

Participants were followed during the anesthetic - surgical procedure, an average of 90 minutes
Total Duration (Dur95%)
Time Frame: Participants were followed during the anesthetic - surgical procedure, an average of 90 minutes

The total duration is the elapsed time for T1 recovery of the response to reach 95% of the initial after the infusion of cisatracurium.

This outcome measure was presented in minutes.

Participants were followed during the anesthetic - surgical procedure, an average of 90 minutes
Spontaneous Recovery (T4/T1=90%)
Time Frame: The participants were followed during the anesthetic - surgical procedure

Spontaneous recovery is the elapsed time for the recovery of the TOF (T4 / T1) response to 90% of the original after infusion of cisatracurium.

This outcome measure was presented in minutes.

The participants were followed during the anesthetic - surgical procedure

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
MAP - M1 (Mean Arterial Pressure in the Moment 1)
Time Frame: This measure of average blood pressure was performed when the patient arrived in the operating room
In the operating room, patients were cardiovascular, respiratory and body temperature monitored through the Dixtal 2020. The mean blood pressure was recorded and annotated at various times such as in the arrival of the patient in the operating room. This time point was named as moment '1'.
This measure of average blood pressure was performed when the patient arrived in the operating room
MAP - M2 (Mean Arterial Pressure in the Moment 2)
Time Frame: This measure of average blood pressure was performed immediately before induction of anesthesia
In the operating room, patients were cardiovascular, respiratory and body temperature monitored through the Dixtal 2020. The mean blood pressure was recorded and annotated at various times such as in the moment immediately before the anesthesia induction. This time point was named as moment '2'.
This measure of average blood pressure was performed immediately before induction of anesthesia
MAP - M3 (Mean Arterial Pressure in the Moment 3)
Time Frame: This measure of average blood pressure was performed immediately before the start of the infusion of the solution X (magnesium sulfate or isotonic solution) and Y solution (lidocaine or isotonic solution)
In the operating room, patients were cardiovascular, respiratory and body temperature monitored through the Dixtal 2020. The mean blood pressure was recorded and annotated at various times such as immediately before the start of the infusion of the solution X (magnesium sulfate or isotonic solution) and Y solution (lidocaine or isotonic solution). This time point was named as moment '3'.
This measure of average blood pressure was performed immediately before the start of the infusion of the solution X (magnesium sulfate or isotonic solution) and Y solution (lidocaine or isotonic solution)
MAP - M4 (Mean Arterial Pressure in the Moment 4)
Time Frame: This measure of average blood pressure was performed five minutes after M3 (in the end of the X and Y solutions infusion)
In the operating room, patients were cardiovascular, respiratory and body temperature monitored through the Dixtal 2020. The mean blood pressure was recorded and annotated at various times such as in the end of the study solutions infusion.This time point was named as moment '4'.
This measure of average blood pressure was performed five minutes after M3 (in the end of the X and Y solutions infusion)
MAP - M5 (Mean Arterial Pressure in the Moment 5)
Time Frame: This measure of average blood pressure was performed immediately before the tracheal intubation
In the operating room, patients were cardiovascular, respiratory and body temperature monitored through the Dixtal 2020. The mean blood pressure was recorded and annotated at various times such as immediately before the tracheal intubation. This time point was named as moment '5'.
This measure of average blood pressure was performed immediately before the tracheal intubation
MAP - M6 (Mean Arterial Pressure in the Moment 6)
Time Frame: This measure of average blood pressure was performed one minute after the tracheal intubation
In the operating room, patients were cardiovascular, respiratory and body temperature monitored through the Dixtal 2020. The mean blood pressure was recorded and annotated at various times such as one minute after the tracheal intubation. This time point was named as moment '6'.
This measure of average blood pressure was performed one minute after the tracheal intubation
HR - M1 (Heart Rate in the Moment 1)
Time Frame: This measure of heart rate was performed when the patient arrived in the operating room
In the operating room, patients were cardiovascular, respiratory and body temperature monitored through the Dixtal 2020. The measure of heart rate was recorded and annotated at various times such as in the arrival of the patient in the operating room. This time point was named as moment '1'.
This measure of heart rate was performed when the patient arrived in the operating room
HR - M2 (Heart Rate in the Moment 2)
Time Frame: This measure of heart rate was performed immediately before induction of anesthesia
In the operating room, patients were cardiovascular, respiratory and body temperature monitored through the Dixtal 2020. The heart rate was recorded and annotated at various times such as in the moment immediately before the anesthesia induction. This time point was named as moment '2'.
This measure of heart rate was performed immediately before induction of anesthesia
HR - M3 (Heart Rate in the Moment 3)
Time Frame: This measure of heart rate was performed immediately before the start of the infusion of the solution X (magnesium sulfate or isotonic solution) and Y solution (lidocaine or isotonic solution)
In the operating room, patients were cardiovascular, respiratory and body temperature monitored through the Dixtal 2020. The heart rate was recorded and annotated at various times such as immediately before the start of the infusion of the solution X (magnesium sulfate or isotonic solution) and Y solution (lidocaine or isotonic solution). This time point was named as moment '3'.
This measure of heart rate was performed immediately before the start of the infusion of the solution X (magnesium sulfate or isotonic solution) and Y solution (lidocaine or isotonic solution)
HR - M4 (Heart Rate in the Moment 4)
Time Frame: This measure of heart rate was performed five minutes after M3 (in the end of the X and Y solutions infusion)
In the operating room, patients were cardiovascular, respiratory and body temperature monitored through the Dixtal 2020. The heart rate was recorded and annotated at various times such as in the end of the study solutions infusion. This time point was named as moment '4'.
This measure of heart rate was performed five minutes after M3 (in the end of the X and Y solutions infusion)
HR - M5 (Heart Rate in the Moment 5)
Time Frame: This measure of heart rate was performed immediately before the tracheal intubation
In the operating room, patients were cardiovascular, respiratory and body temperature monitored through the Dixtal 2020. The heart rate was recorded and annotated at various times such as immediately before the tracheal intubation. This time point was named as moment '5'.
This measure of heart rate was performed immediately before the tracheal intubation
HR - M6 (Heart Rate in the Moment 6)
Time Frame: This measure of heart rate was performed one minute after the tracheal intubation
In the operating room, patients were cardiovascular, respiratory and body temperature monitored through the Dixtal 2020. The heart rate was recorded and annotated at various times such as one minute after the tracheal intubation. This time point was named as moment '6'.
This measure of heart rate was performed one minute after the tracheal intubation
MAP - M7a (Mean Arterial Pressure in the Moment 7a)
Time Frame: This measure of average blood pressure was performed 15 minutes after the traqueal intubation
In the operating room, patients were cardiovascular, respiratory and body temperature monitored through the Dixtal 2020. The mean blood pressure was recorded and annotated at various times such as 15 minutes after the traqueal intubation. This time point was named as moment '7a'.
This measure of average blood pressure was performed 15 minutes after the traqueal intubation
MAP - M7b (Mean Arterial Pressure in the Moment 7b)
Time Frame: This measure of average blood pressure was performed 30 minutes after the traqueal intubation
In the operating room, patients were cardiovascular, respiratory and body temperature monitored through the Dixtal 2020. The mean blood pressure was recorded and annotated at various times such as 30 minutes after the traqueal intubation. This time point was named as moment '7b'.
This measure of average blood pressure was performed 30 minutes after the traqueal intubation
MAP - M7c (Mean Arterial Pressure in the Moment 7c)
Time Frame: This measure of average blood pressure was performed 45 minutes after the traqueal intubation
In the operating room, patients were cardiovascular, respiratory and body temperature monitored through the Dixtal 2020. The mean blood pressure was recorded and annotated at various times such as 45 minutes after the traqueal intubation. This time point was named as moment '7c'.
This measure of average blood pressure was performed 45 minutes after the traqueal intubation
MAP - M7d (Mean Arterial Pressure in the Moment 7d)
Time Frame: This measure of average blood pressure was performed 60 minutes after the traqueal intubation
In the operating room, patients were cardiovascular, respiratory and body temperature monitored through the Dixtal 2020. The mean blood pressure was recorded and annotated at various times such as 60 minutes after the traqueal intubation. This time point was named as moment '7d'.
This measure of average blood pressure was performed 60 minutes after the traqueal intubation
MAP - M7e (Mean Arterial Pressure in the Moment 7e)
Time Frame: This measure of average blood pressure was performed 75 minutes after the traqueal intubation
In the operating room, patients were cardiovascular, respiratory and body temperature monitored through the Dixtal 2020. The mean blood pressure was recorded and annotated at various times such as 75 minutes after the traqueal intubation. This time point was named as moment '7e'.
This measure of average blood pressure was performed 75 minutes after the traqueal intubation
MAP - M7f (Mean Arterial Pressure in the Moment 7f)
Time Frame: This measure of average blood pressure was performed 90 minutes after the traqueal intubation
In the operating room, patients were cardiovascular, respiratory and body temperature monitored through the Dixtal 2020. The mean blood pressure was recorded and annotated at various times such as 90 minutes after the traqueal intubation. This time point was named as moment '7f'.
This measure of average blood pressure was performed 90 minutes after the traqueal intubation
HR - M7a (Heart Rate in the Moment 7a)
Time Frame: This measure of heart rate was performed 15 minutes after the traqueal intubation
In the operating room, patients were cardiovascular, respiratory and body temperature monitored through the Dixtal 2020. The heart rate was recorded and annotated at various times such as 15 minutes after the traqueal intubation.This time point was named as moment '7a'.
This measure of heart rate was performed 15 minutes after the traqueal intubation
HR - M7b (Heart Rate in the Moment 7b)
Time Frame: This measure of heart rate was performed 30 minutes after the traqueal intubation
In the operating room, patients were cardiovascular, respiratory and body temperature monitored through the Dixtal 2020. The heart rate was recorded and annotated at various times such as 30 minutes after the traqueal intubation. This time point was named as moment '7b'.
This measure of heart rate was performed 30 minutes after the traqueal intubation
HR - M7c (Heart Rate in the Moment 7c)
Time Frame: This measure of heart rate was performed 45 minutes after the traqueal intubation
In the operating room, patients were cardiovascular, respiratory and body temperature monitored through the Dixtal 2020. The heart rate was recorded and annotated at various times such as 45 minutes after the traqueal intubation. This time point was named as moment '7c'.
This measure of heart rate was performed 45 minutes after the traqueal intubation
HR - M7d (Heart Rate in the Moment 7d)
Time Frame: This measure of heart rate was performed 60 minutes after the traqueal intubation
In the operating room, patients were cardiovascular, respiratory and body temperature monitored through the Dixtal 2020. The heart rate was recorded and annotated at various times such as 60 minutes after the traqueal intubation. This time point was named as moment '7d'.
This measure of heart rate was performed 60 minutes after the traqueal intubation
HR - M7e (Heart Rate in the Moment 7e)
Time Frame: This measure of heart rate was performed 75 minutes after the traqueal intubation
In the operating room, patients were cardiovascular, respiratory and body temperature monitored through the Dixtal 2020. The heart rate was recorded and annotated at various times such as 75 minutes after the traqueal intubation. This time point was named as moment '7e'.
This measure of heart rate was performed 75 minutes after the traqueal intubation
HR - M7f (Heart Rate in the Moment 7f)
Time Frame: This measure of heart rate was performed 90 minutes after the traqueal intubation
In the operating room, patients were cardiovascular, respiratory and body temperature monitored through the Dixtal 2020. The heart rate was recorded and annotated at various times such as 90 minutes after the traqueal intubation. This time point was named as moment '7f'.
This measure of heart rate was performed 90 minutes after the traqueal intubation

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

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General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

July 1, 2015

Primary Completion (Actual)

August 1, 2015

Study Completion (Actual)

September 1, 2015

Study Registration Dates

First Submitted

June 18, 2015

First Submitted That Met QC Criteria

June 24, 2015

First Posted (Estimate)

June 29, 2015

Study Record Updates

Last Update Posted (Estimate)

January 15, 2016

Last Update Submitted That Met QC Criteria

December 10, 2015

Last Verified

December 1, 2015

More Information

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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