- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03580720
Electromyography for Diaphragm Effort (Edi2Pdi)
Diaphragm Electromyography to Estimate Breathing Effort: a Physiological Study
Mechanical ventilation may be necessary to save the life of a patient due to an accident, pneumonia or surgery. The ventilator then temporarily takes over the function of the respiratory muscles. During treatment in the Intensive Care, the amount of support provided by the ventilator is usually lowered gradually, until the point that the patient can breathe unassisted once again. However, in a large fraction of patients (up to 40%) it takes days to weeks before the patient is able to breathe unassisted, even after the initial disease has been treated. This is called prolonged weaning.
A possible cause of prolonged weaning is weakness of the respiratory muscles. The diaphragm, the largest respiratory muscle, can become weakened if it is used too little, much like all other muscles in the body. Additionally, damage and weakness of the diaphragm can occur when the diaphragm has to work excessively. Therefore, it is important that the diaphragm works enough; not so little that it becomes weakened, but not too much either.
Measurements of pressure generated by the diaphragm are needed to determine the current level of diaphragm activity in a patient on mechanical ventilation. However, these measurements are rarely performed, because they are time-consuming and require placement of two additional nasogastric catheters. This is a shame, as adequate loading of the diaphragm might prevent development of weakness, leading to shorter duration of mechanical ventilation. Finding alternative measurements of diaphragm effort might be a solution to this problem.
It has been hypothesized that the electrical activity of the diaphragm provides a reliable indication of diaphragm effort. This study aims to determine whether there is a correlation between pressure generation by the diaphragm and electrical activity of the diaphragm over a wide range of respiratory activity, from low effort to extreme effort, in healthy volunteers.
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Noord-Holland
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Amsterdam, Noord-Holland, Netherlands, 1081HV
- Amsterdam UMC, location VUmc
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Informed Consent
- Age >18 years
Exclusion Criteria:
- History of cardiac and/or pulmonary disease or current medication use
- History of pneumothorax
- Contra-indications for nasogastric tube placement (recent epistaxis, severe coagulopathy, current upper airway pathology)
- Contra-indication for magnetic stimulation (cardiac pacemakers or metal in cervical area)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Intervention
Intervention group, receiving Inspiratory threshold loading protocol.
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Subjects will be instrumented with catheters that measure electrical activity of the diaphragm and transdiaphragmatic pressure.
Subjects will perform a stepwise inspiratory threshold loading protocol to induce a wide range of diaphragm activity.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Electrical activity of the diaphragm
Time Frame: Electrical activity of the diaphragm will be assessed at multiple levels of breathing effort in each subject for two hours.
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Diaphragm electromyography will be obtained with multiple electrode pairs situated on specialized esophageal catheters.
The raw diaphragm electromyography will be filtered and integrated to obtain the compound mean action potential reported in microvolts (μV) as described in ref 1 (Sinderby et al.).
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Electrical activity of the diaphragm will be assessed at multiple levels of breathing effort in each subject for two hours.
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Transdiaphragmatic pressure
Time Frame: Transdiaphragmatic pressure will be assessed at multiple levels of breathing effort in each subject for two hours.
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The pressure gradient over the diaphragm will be obtained by subtracting the esophageal pressure from the pressure in the stomach, measured with specialized catheters, and will be reported in centimeters of water (cmH2O) as described in ref 3, American Thoracic Society (ATS) statement on respiratory muscle testing.
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Transdiaphragmatic pressure will be assessed at multiple levels of breathing effort in each subject for two hours.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Work of breathing
Time Frame: Work of breathing will be assessed at multiple levels of breathing effort in each subject for two hours.
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Work of breathing will be obtained by integrating the pressure-volume loops of esophageal pressure and tidal volume, and will be reported in Joule per minute as described in ref 3, ATS statement on respiratory muscle testing..
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Work of breathing will be assessed at multiple levels of breathing effort in each subject for two hours.
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Pressure-time product of the diaphragm
Time Frame: Pressure-time product of the diaphragm will be assessed at multiple levels of breathing effort in each subject for two hours.
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Pressure-time product of the diaphragm will be obtained by dividing the time-integral of transdiaphragmatic pressure (described above) over time, and will be reported as cmH20*s per minute as described in ref 3, ATS statement on respiratory muscle testing..
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Pressure-time product of the diaphragm will be assessed at multiple levels of breathing effort in each subject for two hours.
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Pressure-time product of the respiratory muscles
Time Frame: Pressure-time product of the respiratory muscles will be assessed at multiple levels of breathing effort in each subject for two hours.
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Pressure-time product of the respiratory muscles will be obtained by dividing the time-integral of esophageal pressure over time, and will be reported as cmH20*s per minute as described in ref 3, ATS statement on respiratory muscle testing..
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Pressure-time product of the respiratory muscles will be assessed at multiple levels of breathing effort in each subject for two hours.
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Mechanical power
Time Frame: Mechanical power will be assessed at multiple levels of breathing effort in each subject for two hours.
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Mechanical power will be obtained by multiplying the work of breathing (described above) by the number of breaths per minute, and will be reported in Watt (joule/minute) as described in ref 3, ATS statement on respiratory muscle testing..
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Mechanical power will be assessed at multiple levels of breathing effort in each subject for two hours.
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Accessory muscle recruitment
Time Frame: Two hours.
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As an explorative end-point, the timepoint at which several accessory inspiratory muscles are recruited during incremental respiratory loading will be studied and reported (if technically possible)
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Two hours.
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Diaphragm thickening fraction.
Time Frame: Thickening fractions will be obtained at multiple levels of breathing effort in each subject for up to two hours
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Using a linear probe positioned in the mid-axillary line the diaphragm will be visualized as per clinical protocol.
Diaphragm thickness will be measured during inspiration and expiration and will be reported in mm.
Thickening fraction will be obtained with the following formula: (Thickness during inspiration - thickness during expiration) / thickness during expiration * 100% as described in ref 2 (Vivier et al.).
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Thickening fractions will be obtained at multiple levels of breathing effort in each subject for up to two hours
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Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Angelique Spoelstra - de Man, MD, PhD, Amsterdam UMC, location VUmc
- Principal Investigator: Leo Heunks, MD, PhD, Amsterdam UMC, location VUmc
Publications and helpful links
General Publications
- Vivier E, Mekontso Dessap A, Dimassi S, Vargas F, Lyazidi A, Thille AW, Brochard L. Diaphragm ultrasonography to estimate the work of breathing during non-invasive ventilation. Intensive Care Med. 2012 May;38(5):796-803. doi: 10.1007/s00134-012-2547-7. Epub 2012 Apr 5.
- American Thoracic Society/European Respiratory Society. ATS/ERS Statement on respiratory muscle testing. Am J Respir Crit Care Med. 2002 Aug 15;166(4):518-624. doi: 10.1164/rccm.166.4.518. No abstract available.
- Sinderby CA, Beck JC, Lindstrom LH, Grassino AE. Enhancement of signal quality in esophageal recordings of diaphragm EMG. J Appl Physiol (1985). 1997 Apr;82(4):1370-7. doi: 10.1152/jappl.1997.82.4.1370.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- NL64648.029.18
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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