Mechanical Ventilation Controlled by the Electrical Activity of the Patient's Diaphragm - Effects on Cardiac Performance
Primary Purpose
Respiratory Failure, Cardiac Failure
Status
Completed
Phase
Phase 1
Locations
Switzerland
Study Type
Interventional
Intervention
Neurally adjusted ventilatory assist (NAVA) provided by a commercially available mechanical ventilator (Servo i, Maquet Critical Care, Solna, Sweden).
Sponsored by
About this trial
This is an interventional treatment trial for Respiratory Failure focused on measuring respiratory insufficiency, respiration, ventilators, diaphragm, electromyography, mechanical ventilation
Eligibility Criteria
Inclusion Criteria:
- Male or female patients aged 18 - 85 years (extremes included)
- Mechanical ventilation (tracheally intubated or tracheotomized)
Relevant interaction between the ventilator and the cardiac performance defined as an inspiratory deflection in central venous pressure or pulmonary diastolic pressure of ≥ 5 mmHg
in 10 patients with impaired cardiac performance defined as either
- a left ventricular ejection fraction of < 40% and/or
- treatment with dobutamine ≥2μg/kg/min, or adrenaline ≥ 3μg/kg/min and/or
- a cardiac index of ≤ 2.2 L•min-1•m2 and/or
- a pulmonary artery occlusion pressure (PAOP) ≥ 18 mmHg
in 10 patients with a history of chronic obstructive pulmonary disease (COPD) and delayed triggering-ON / cycling-OFF and/or evidence for wasted inspiratory efforts as evidenced by:
- limitation of expiratory air flow and intrinsic PEEP as assessed by observation of the expiratory air flow curve and measurement of the airway pressure during an expiratory hold maneuver and/or
- excessive activation of inspiratory and / or expiratory muscles as assessed by observation of the patient
- Presence of a pulmonary artery catheter and an arterial pressure line
- Subject itself or its next of kin has given written informed consent
Exclusion Criteria:
- Patient is less than 18 years or more than 80 years of age
- The attending physician refuses to allow enrollment
- The patient refuses informed consent
- Next of kin is unavailable or refuses informed consent
- Pregnant or breast-feeding female. A pregnancy test will be performed in all female patients less than 60 years of age. The patient will not be enrolled in the study if the test result is positive.
- Any contraindication to insertion/exchange a nasogastric tube, including (but not limited to): severe oropharyngeal malformation or bleeding; esophageal varices, tumor, infection, stenosis, or rupture
- Presence or suspicion of diaphragm injury
- Hemophilia or other severe bleeding disorder
- Presence or suspicion of a central nervous system (CNS) disorder, including (but not limited to): CNS infarction, bleeding, tumor, or infection
- History of heart and/or lung transplantation
- Any mechanical cardiac assist device (including intraaortic balloon pump)
- Any contraindication to reduce sedation or to stop neuromuscular blockage in order to allow spontaneous breathing
- The patient needs to be ventilated with a mode of MV controlling for tidal volume or for airway pressure as per attending physician.
- Severe hemodynamic instability as judged by the attending physician
- Planned or anticipated intervention within the study period necessitating either transfer out of the ICU or requiring prolonged interaction with the patient.
- a fraction of inspired oxygen (FiO2) of > 0.8
- The patient currently participates in another interventional clinical trial
Sites / Locations
- Department of Intensive Care Medicine, University Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
NAVA
Arm Description
Outcomes
Primary Outcome Measures
Cardiac stroke volume index.
Secondary Outcome Measures
Global delivery of oxygen
Full Information
NCT ID
NCT00647361
First Posted
March 19, 2008
Last Updated
July 18, 2011
Sponsor
Insel Gruppe AG, University Hospital Bern
1. Study Identification
Unique Protocol Identification Number
NCT00647361
Brief Title
Mechanical Ventilation Controlled by the Electrical Activity of the Patient's Diaphragm - Effects on Cardiac Performance
Official Title
Short Term Effects of Neurally Adjusted Ventilatory Assist and Pressure Support Ventilation on Cardiac Performance
Study Type
Interventional
2. Study Status
Record Verification Date
July 2011
Overall Recruitment Status
Completed
Study Start Date
March 2008 (undefined)
Primary Completion Date
June 2010 (Actual)
Study Completion Date
June 2010 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Insel Gruppe AG, University Hospital Bern
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Neurally adjusted ventilatory assist (NAVA) is a new concept of mechanical ventilation. NAVA delivers assist to spontaneous breathing based on the detection of the electrical activity of the diaphragm. We study the effect of NAVA on cardiac performance in critically ill, mechanically ventilated patients.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Respiratory Failure, Cardiac Failure
Keywords
respiratory insufficiency, respiration, ventilators, diaphragm, electromyography, mechanical ventilation
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
15 (Actual)
8. Arms, Groups, and Interventions
Arm Title
NAVA
Arm Type
Experimental
Intervention Type
Device
Intervention Name(s)
Neurally adjusted ventilatory assist (NAVA) provided by a commercially available mechanical ventilator (Servo i, Maquet Critical Care, Solna, Sweden).
Intervention Description
Neurally adjusted ventilatory assist (NAVA) and pressure support ventilation (PSV)
Primary Outcome Measure Information:
Title
Cardiac stroke volume index.
Time Frame
end of experimental periods
Secondary Outcome Measure Information:
Title
Global delivery of oxygen
Time Frame
end of experimental period
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Male or female patients aged 18 - 85 years (extremes included)
Mechanical ventilation (tracheally intubated or tracheotomized)
Relevant interaction between the ventilator and the cardiac performance defined as an inspiratory deflection in central venous pressure or pulmonary diastolic pressure of ≥ 5 mmHg
in 10 patients with impaired cardiac performance defined as either
a left ventricular ejection fraction of < 40% and/or
treatment with dobutamine ≥2μg/kg/min, or adrenaline ≥ 3μg/kg/min and/or
a cardiac index of ≤ 2.2 L•min-1•m2 and/or
a pulmonary artery occlusion pressure (PAOP) ≥ 18 mmHg
in 10 patients with a history of chronic obstructive pulmonary disease (COPD) and delayed triggering-ON / cycling-OFF and/or evidence for wasted inspiratory efforts as evidenced by:
limitation of expiratory air flow and intrinsic PEEP as assessed by observation of the expiratory air flow curve and measurement of the airway pressure during an expiratory hold maneuver and/or
excessive activation of inspiratory and / or expiratory muscles as assessed by observation of the patient
Presence of a pulmonary artery catheter and an arterial pressure line
Subject itself or its next of kin has given written informed consent
Exclusion Criteria:
Patient is less than 18 years or more than 80 years of age
The attending physician refuses to allow enrollment
The patient refuses informed consent
Next of kin is unavailable or refuses informed consent
Pregnant or breast-feeding female. A pregnancy test will be performed in all female patients less than 60 years of age. The patient will not be enrolled in the study if the test result is positive.
Any contraindication to insertion/exchange a nasogastric tube, including (but not limited to): severe oropharyngeal malformation or bleeding; esophageal varices, tumor, infection, stenosis, or rupture
Presence or suspicion of diaphragm injury
Hemophilia or other severe bleeding disorder
Presence or suspicion of a central nervous system (CNS) disorder, including (but not limited to): CNS infarction, bleeding, tumor, or infection
History of heart and/or lung transplantation
Any mechanical cardiac assist device (including intraaortic balloon pump)
Any contraindication to reduce sedation or to stop neuromuscular blockage in order to allow spontaneous breathing
The patient needs to be ventilated with a mode of MV controlling for tidal volume or for airway pressure as per attending physician.
Severe hemodynamic instability as judged by the attending physician
Planned or anticipated intervention within the study period necessitating either transfer out of the ICU or requiring prolonged interaction with the patient.
a fraction of inspired oxygen (FiO2) of > 0.8
The patient currently participates in another interventional clinical trial
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lukas Brander, MD
Organizational Affiliation
Department of Intensive Care Medicine, University Hospital - Inselspital, Bern, Switzerland
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Intensive Care Medicine, University Hospital
City
Bern
ZIP/Postal Code
3010
Country
Switzerland
12. IPD Sharing Statement
Citations:
PubMed Identifier
10581089
Citation
Sinderby C, Navalesi P, Beck J, Skrobik Y, Comtois N, Friberg S, Gottfried SB, Lindstrom L. Neural control of mechanical ventilation in respiratory failure. Nat Med. 1999 Dec;5(12):1433-6. doi: 10.1038/71012. No abstract available.
Results Reference
background
PubMed Identifier
25212533
Citation
Berger D, Bloechlinger S, Takala J, Sinderby C, Brander L. Heart-lung interactions during neurally adjusted ventilatory assist. Crit Care. 2014 Sep 12;18(5):499. doi: 10.1186/s13054-014-0499-8.
Results Reference
derived
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Mechanical Ventilation Controlled by the Electrical Activity of the Patient's Diaphragm - Effects on Cardiac Performance
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