Recovery of Muscle Function After Deep Neuromuscular Block by Means of Diaphragm Ultrasonography

October 24, 2016 updated by: Dr. Chiara Adembri, University of Florence

Recovery of Muscle Function After Deep Neuromuscular Block by Means of Dia-phragm Ultrasonography and Adductor Pollicis Acceleromyography: Comparison of Neostigmine vs. Sugammadex as Reversal Drugs.

Diaphragm ultrasonography as a diagnostic tool in order to demonstrate the superiority of Sugammadex vs. AChEI in facilitating post-operative neuromuscular recovery.

Study Overview

Status

Unknown

Conditions

Intervention / Treatment

Detailed Description

The proposed study will be a prospective, double-blind, single center randomized study performed in 60 patients with ASA physical status I-II, between 18-80 years old, undergoing dNMB with rocuronium during ear nose and throat (ENT) surgery. Randomization will be performed using a table created from the website www.randomization.com, and patients will be divided equally into two groups: Treatment with Sugammadex (SUG group) or treatment with Neostigmine (NEO group). Exclusion criteria will include: A history of hepatic or renal disease, chron-ic or acute alcoholism, allergy or hypersensitivity to Sugammadex and/or atropine or Neostigmine, current medications with CNS effects, a history of neurologic disease, diaphragmatic palsy, pregnancy or nursing arrhythmias. Continuous neuromuscular monitoring will be performed using TOF ratios obtained from ad-ductor pollicis muscle. At the conclusion of the surgical procedure, patients will receive either Neostigmine (NEO group) or Sugammadex (SUG group) for NMB reversal. The physician who will administer the study drugs will insure that is per-formed on an open-label (non-blinded) basis. All patients showing a TOF ratio ≥0.9 will be extubated. Diaphragmatic function (assessed by ultrasonographic evaluation of the TF and amplitude of excursion) will be evaluated in each subject at the following time points:

  1. Prior to induction of general anesthesia.
  2. At the conclusion of the surgical procedure when TOF ratio is 0.9.
  3. 15 and 30 minutes after discharge from the operating theatre. The physician who will perform the ultrasound scan will be different from the one who involved with administration of the drug for NMB reversal and the former will be blinded with respect to treatment received by patients. It is likely that, despite a TOF value greater than 0.9, higher diaphragm recovery will occur earlier and last longer when reversal of the NMB is achieved using Sugammadex (a specific antagonist) when compared with Neostigmine (a non-specific reversal).

In order to standardize the anesthetic technique, no premedication will be administered to any patient candidate to undergo to microlaryngoscopy procedure. Besides each individual enrolled will receive neuromuscular monitoring with ulnar nerve stimulation with TOF Watch® (Organon, Oss, Netherlands). The device will be calibrated pre-operatively and parameters set using standard train of four (TOF) methodology after administration of hypnotic drug prior to muscle relaxation. Standard induction of general anesthesia will be performed using intravenous (iv) fentanyl (2 mcg kg-1), propofol (2 mg kg-1), and rocuronium (0.6 mg kg-1). Tracheal intubation will be performed when the patient fails to register signals with TOF. Rocuronium (0.15 mg kg-1) will be re-administered when PTC elicits more than 5 twitches in order to maintain a dNMB. Sevoflurane will be administered at1.0 MAC in an air/oxygen mixture. Fentanyl will be titrated with a bolus of 0.5 mcg kg-1 every 30 minutes to maintain analgesia. Prior to induction of anesthesia, ultrasonography diaphragm evaluation will be performed using an ESAOTE ultrasound machine (ESAOTE MyLab, Genova, Italy) by assessing the TF and amplitude of excursion. With the spontaneously breathing patient in semi-recumbent position, the amplitude of excursion will be evaluated following the method of Kim et al (7) using a 3.5-MHz ultrasound probe placed over the intercostal space above the 10th rib in the right mid-axillary line for the right diaphragm and the left mid-axillary line for the left diaphragm. The liver or spleen will be used as a window for each hemi-diaphragm. A two-dimensional mode will be used to find the best approach and to select the exploration line of each hemi-diaphragm. With the probe fixed on the chest wall during respiration, the ultrasound beam will be directed to the hemi-diaphragmatic domes at an angle of not less than 70°. During inspiration, the normal diaphragm contracts and moves caudally toward the transducer; this will be recorded as an upward motion of the M-mode tracing. The amplitude of excursion will be measured on the vertical axis of the tracing from the baseline to the point of maximum height of inspiration on the graph. Three measurements will be performed for each patient and averaged for each side at each time point of the protocol (7). Moreover, TF will be assessed following the method of Vivier et al (6) with a linear high frequency probe set at 12 Mhz. The diaphragm will be located with same method described above and the zone of apposition will assessed at 0.5-2 cm below the costophrenic sinus. The inferior border of the costophrenic sinus will be identified at end-inspiration as the zone of transition from the artifact representation of normal lung (the lung sliding) to the visualization of diaphragm and liver.

The diaphragm thickness will be recorded in time motion (TM) mode. The diaphragm will be outlined using the two clear bright parallel lines of the pleural and peritoneal membranes. Measurements will be averaged out of three or more consecutive breaths on the last valid image recorded at the end of each period (6) .At the conclusion of the surgical procedure and when TOF neuromuscular monitoring shows a minimum of 2 twitches, patients will randomly receive, as described above, either (NEO Group) iv Neostigmine 50 µg kg-1 and atropine 15 µg kg-1 or (SUG group) iv Sugammadex 2 mg kg-1 to reverse residual curarization. Extubation will be performed when all of the following criteria are met: Patient is awake and executes simple commands, shows regular respiratory pattern with a tidal volume of 6-7 mL/kg referred to ideal body weight (IBW) and a TOF ratio ≥0.9. During the period preceding a TOF ratio > 0.9 , bilateral diaphragm ultrasonography evaluating amplitude of excursion and TF will be performed to assess muscle recovery in spontaneous breathing patients. These measurements will be compared with baseline muscle assessment. Three additional diaphragm ultrasound scans will be performed 15 and 30 minutes after discharge from operating theatre. Follow up will be performed to document every adverse event and complication that occurs until discharge from the hospital.

Data will be collected by the use of paper CRF pages. Data entry will be performed at one central site that will maintain the overall database and will perform and be responsible for the data analysis.

The study will be conducted within 8 months -1 year from approval from our ethical committee. A preliminary report will be completed and submitted after the first six months of data collection.

Data will be collected by the use of paper CRF pages. Data entry will be performed at one central site that will maintain the overall database and will perform and be responsible for the data analysis. All the compiled CRFs will be archived. In order to eliminate possible data entry errors, individual data will be compared to a range of plausible values. After data entry, automated checks, that are defined beforehand (a priori), will be performed to evaluate internal inconsistencies, range errors, or missing data. For each atypical/out-of-range/missing data, a query will be automatically sent to the investigator. Once all the queries are solved, the database will be locked and used for statistical analysis.Statistical analysis will be performed in collaboration by the Department of Statistics of the University of Florence. Complete data will not be unblinded until the external medical and statistics review have been completed.

Data will be collected and a single statistical analysis will be performed at the completion of the study using an intention to treat (ITT) analysis. With regard to the primary endpoint, differences between the two groups with respect to distribution of muscle function recovery after deep muscular blockade will be subjected to non-parametric tests depending on the characteristics of outcome distribution. To compare the primary endpoint between the 2 groups, the data will be analysed using Wilcoxon rank sum test for two independent samples as they are expected to be continuous and not normally distributed. As a sensitivity analysis, parametric tests will potentially be employed after thorough evaluation of the validity distribution assumptions.

The ultrasonography and TOF data will be summarized by drug treatment group as mean, standard deviation, quintiles, and minim and maximum values. In addition, two-sided 95% confidence intervals will be calculated on the comparison between the two groups for the main descriptive parameters of the primary and secondary variables.

In order to compare the different percentage of respiratory events in the two arms studied, a chi square test will be performed.

Finally, descriptive statistics of all variables describing characteristics of the patients enrolled in the study and of patients excluded from the study will be produced. The mean, median, standard deviation and range will be calculated for continuous data by drug treatment group. For categorical variables, frequency counts and percentages will be calculated.

Power/Sample Size:

Because this is the first clinical trial that proposes to evaluate this endpoint, no published data are available at this time. However, assuming a 25% of difference of TF between groups would be clinically meaningful, a confidence interval of 95% and power 80%, sample size calculation provided by StatCalc EPI INFO ver 7.0 (Center for Diseases Control, Atlanta, GA, USA) considered 28 patients for each group fundamental to reach the endpoint predefined. This proposal requests funding for a pilot study, with a double blind design, where participants will be randomly enrolled to receive Sugammadex or Neostigmine with a 1:1 allocation using the standardized table created with the website www.randomization.com.

Study Type

Interventional

Enrollment (Anticipated)

58

Phase

  • Phase 4

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Italy
      • Florence, Italy, 50134
        • Recruiting
        • Azienda Ospdaliero Universitaria Careggi
        • Contact:
        • Contact:
        • Principal Investigator:
          • Chiara Adembri, MD
        • Sub-Investigator:
          • Iacopo Cappellini, MD
        • Sub-Investigator:
          • Daniele Ostento, MD
        • Sub-Investigator:
          • Fabio Picciafuochi, MD

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 80 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • ASA physical status I-II
  • age between 18-80 years old
  • dNMB with rocuronium during ear nose and throat (ENT) surgery

Exclusion Criteria:

  • Clinical diagnosis of hepatic or renal disease
  • Clinical diagnosis of chronic or acute alcoholism
  • History of allergy or hypersensitivity to Sugammadex and/or atropine or Neostigmine
  • Current medications with CNS effects
  • History of neurologic disease
  • Diaphragmatic palsy
  • Pregnancy or nursing
  • History of malignant 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

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Sugammadex
patients enrolled who will receive sugammadex 2 mg*kg-1 at the end of surgery
Drug: Sugammadex
Other Names:
  • Bridion
Device: Diaphragm Ultrasonography
Prior to induction of anesthesia each enrolled patients, ultrasonography diaphragm evaluation will be performed using an ESAOTE ultrasound machine (ESAOTE MyLab, Genova, Italy) by assessing the TF and amplitude of excursion.
Other Names:
  • Diaphragm Ultrasound
Device: Neurumuscual monitoring
Neuromuscular monitoring assesses muscle recovery after deep neuromuscular block through trainf of four and post tetanic count method
Other Names:
  • Train of Four and post tetanic count
Drug: Rocuronium
Rocuronium will be administered 0.6 mg*kg-1 to reach neuromuscular block at the induction of general anesthesia and 0.15 mg*kg-1 when PTC elicits more than 5 twitches in order to maintain a deep neuromuscular block
Other Names:
  • Esmeron
Drug: Fentanyl
Fentanest will be administered 2 mcg*kg-1 at the induction of general anesthesia and titrated 0.5 mcg*kg-1 every 30 minutes
Other Names:
  • Fentanest
Drug: Propofol
Propofol will be administered 2 mg*kg-1 at the induction of general anesthesia
Other Names:
  • Diprivan
Drug: Sevoflurane
Sevoflurane will be administered at 1.0 MAC in an air/oxygen mixture
Other Names:
  • Sevorane
Active Comparator: Nestigmine, Atropine
patients enrolled who will receive neostigmine 50 mcg*kg-1 and atropine 15 mcg*kg-1 at the end of surgery
Drug: Neostigmine
Other Names:
  • Prostigmin
Drug: Atropine
Device: Diaphragm Ultrasonography
Prior to induction of anesthesia each enrolled patients, ultrasonography diaphragm evaluation will be performed using an ESAOTE ultrasound machine (ESAOTE MyLab, Genova, Italy) by assessing the TF and amplitude of excursion.
Other Names:
  • Diaphragm Ultrasound
Device: Neurumuscual monitoring
Neuromuscular monitoring assesses muscle recovery after deep neuromuscular block through trainf of four and post tetanic count method
Other Names:
  • Train of Four and post tetanic count
Drug: Rocuronium
Rocuronium will be administered 0.6 mg*kg-1 to reach neuromuscular block at the induction of general anesthesia and 0.15 mg*kg-1 when PTC elicits more than 5 twitches in order to maintain a deep neuromuscular block
Other Names:
  • Esmeron
Drug: Fentanyl
Fentanest will be administered 2 mcg*kg-1 at the induction of general anesthesia and titrated 0.5 mcg*kg-1 every 30 minutes
Other Names:
  • Fentanest
Drug: Propofol
Propofol will be administered 2 mg*kg-1 at the induction of general anesthesia
Other Names:
  • Diprivan
Drug: Sevoflurane
Sevoflurane will be administered at 1.0 MAC in an air/oxygen mixture
Other Names:
  • Sevorane

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Number of participants with post-operative residual curarization (PORC) as assessed by diaphragm ultrasonography in order to determine its muscle strenght
Time Frame: 30 minutes from the end of surgical procedure
The clinician will assess TF (defined as a percentage) and amplitude of excursion (expressed in millimetres) of the diaphragm by means of ultrasonography
30 minutes from the end of surgical procedure

Secondary Outcome Measures

Outcome Measure
Time Frame
Number of participants with post-operative complications related to PORC such as pneumonia as assessed chest x ray, drop of SpO2 by means of pulse oximeter and blood gas sample.
Time Frame: up to 1 week
up to 1 week
Number of participants with post-operative nausea and vomiting (PONV) as assessed by postoperative nause and vomiting visual analogic scale (PONV VAS)
Time Frame: up to 48 hours
up to 48 hours

Collaborators and Investigators

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

Sponsor

University of Florence

Collaborators

Merck Sharp & Dohme LLC

Investigators

  • Principal Investigator: Chiara Adembri, MD, University of Florence

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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

November 1, 2014

Primary Completion (Anticipated)

February 1, 2017

Study Completion (Anticipated)

July 1, 2017

Study Registration Dates

First Submitted

February 15, 2016

First Submitted That Met QC Criteria

February 27, 2016

First Posted (Estimate)

March 4, 2016

Study Record Updates

Last Update Posted (Estimate)

October 25, 2016

Last Update Submitted That Met QC Criteria

October 24, 2016

Last Verified

October 1, 2016

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • EUDRACT 2013-004-787-62

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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