Ventil Device Usefulness in Mechanically Ventilated ICU Patients
Primary Purpose
Respiratory Insufficiency
Status
Unknown status
Phase
Not Applicable
Locations
Poland
Study Type
Interventional
Intervention
Ventil - a gas flow divider
Sponsored by
About this trial
This is an interventional other trial for Respiratory Insufficiency focused on measuring critically ill patient, intensive care unit, mechanical ventilation, pandemic
Eligibility Criteria
Inclusion Criteria:
- ICU patients who require mechanical ventilation
Exclusion Criteria:
- Patients who require complex modes of ventilation will not be recruited
The sudy in an individual patient be discontinued if case of:
Respiratory Criteria:
- episodes of desaturation <90% (in pts without COPD) without reversibel reason
- need for FiO2 increase by 10%
- need for switch to other than CMV mode of ventillation
- need for neuromucular blockade or for deepen sedation because of assynchrony between patient and venilator
- cummulation of CO2>45 mm Hg (in pts without COPD) not responding to the increase of minute ventilation for 30 minutes
- Pplat >30 cmH2O
Circulatory criteria:
New haemodynamic disturbances that cannot be explaned by other reasons
- ↑ or ↓of BP by 20%
- ↑ or ↓of HR by 20%
- clinically important heart rhythm disturbances
Sites / Locations
- Medical University of GdanskRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
mechanically ventilated patients
Arm Description
Adult ICU patients who are mechanically ventilated and who do not require complex modes of ventilation. A designated flow divider (Ventil) will be used to divide inspiratory gas flow from ventilator in two separate streams - one to the patient and the second to the artificial lung
Outcomes
Primary Outcome Measures
Number of cases in which it was necessary to stop using Ventil and to step- back to ventilation without this flow divider
Ventil will be removed from the patient-ventilator circiuit in case of episodes of desaturation <90% (in pts without COPD) without reversibel reason; need for FiO2 increase by 10%; need for switch to other than CMV mode of ventillation need for neuromucular blockade or for deepen sedation because of assynchrony between patient and venilator cummulation of CO2>45 mm Hg (in pts without COPD) not responding to the increase of minute ventilation for 30 minutes; if Pplat >30 cmH2O; in case of new haemodynamic disturbances that cannot be explaned by other reasons; in case of increase or decrease of BP by 20%; increase or decrease of HR by 20%; in case of occurence of clinically important heart rhythm disturbances
Secondary Outcome Measures
Full Information
NCT ID
NCT04355754
First Posted
April 16, 2020
Last Updated
April 23, 2020
Sponsor
Medical University of Gdansk
Collaborators
Ministry of Science and Higher Education, Poland
1. Study Identification
Unique Protocol Identification Number
NCT04355754
Brief Title
Ventil Device Usefulness in Mechanically Ventilated ICU Patients
Official Title
Assesment of Usefulness of Ventil Device for Mechanical Ventilation in ICU Patients
Study Type
Interventional
2. Study Status
Record Verification Date
April 2020
Overall Recruitment Status
Unknown status
Study Start Date
April 15, 2020 (Actual)
Primary Completion Date
May 2020 (Anticipated)
Study Completion Date
December 31, 2020 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Medical University of Gdansk
Collaborators
Ministry of Science and Higher Education, Poland
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
During Covid-19 pandemic many patients require mechanical ventilation due to disastrous impact of SARS-CoV-2 on lungs. In several countries there is a shortage of ICU beds and ventilators. Critically ill patients are treated outside ICUs. Doctors are facing ethical dilemmas who they should treat with ventilation, who should receive ventilator and who should but will not. In ICUs or step down units or in nursery homes there are also patients beyond hope treated - very often they are dependent on mechanical ventilation. Some attempts to invent a device that could replace complex machines in patients with anticipated poor outcome have been made. Ventil was used in clinical scenarios for separate lung ventilation with good effect. As a flow divider it has a potential to ventilate 2 patients at the same time. In the study Ventil will ventilate one patient and instead of the second there will be an artificial lung. Tidal volumes, minute ventilation, PEEP set and final will be checked. Ppeak, Pmean, Pplat, Cdyn, airway resistance, EtCO2, Sat O2, HR, SAP, DAP will be monitored every 2 hrs, as well as blood-gas analysis (every 8 hrs).
Detailed Description
During Covid-19 pandemic many patients require mechanical ventilation due to disastrous impact of SARS-CoV-2 on lungs. In several countries there is a shortage of ICU beds and ventilators. Critically ill patients are treated outside ICUs. Doctors are facing ethical dilemmas who they should treat with ventilation, who should receive ventilator and who should but will not.
Before pandemic in ICUs there had always been patients who required mechanical ventilation because of extrapulmonary reasons as well as palliative cases or those in vegetative condition. Most of these patients require just a simple ventilator, not a sophisticated mode of ventilation. Some attempts to invent a device that could replace complex machines in patients with anticipated poor outcome have been made. Ventil was used in clinical scenarios for separate lung ventilation with good effect. VENTIL device, a flow divider, theoretically allows for independent, fully automated synchronous ventilation of 2 patients with use of only one respirator. In the shortage of respirators (ex. terrorist attack, natural disasters) device allows also to ventilate in classical system two patients using single respirator.
Ventil - independent lung ventilation system was constructed by engineers from Nalecz Institute of Biocybernetics and Biomedical Engineering of Polish Academy of Science. Ventil was tested in the clinical scenario - it's safety had been confirmed. Several years ago the working prototypes of the device, after approval of Ethical Committee, was tested in about 150 patients, who were ventilated with independent synchronous lung ventilation and had been found useful.
The idea of the study is to check the usefulness of the device (modern version) in ICU patients who can be ventilated with volume -controlled mode of ventilation as an attempt to use single device for ventilation of 2 patients. At this moment, according to several scientific societies, sharing mechanical ventilators should not be attempted because it cannot be done safely with current equipment. However, it is possible that using a designed flow divider will allow safe ventilation in patients without needs for complicated modes of ventilation. Then maybe it will be possible to release some ventilators and to use them in patients in severe condition, mainly in the era of extreme ventilator shortage. In the study Ventil will ventilate one patient and instead of the second, there will be an artificial lung. Tidal volumes, minute ventilation, PEEP set and final will be checked. Ppeak, Pmean, Pplat, Cdyn, airway resistance, EtCO2, Sat O2, HR, SAP, DAP will be monitored (every 2 hrs), as well as blood-gas analysis (every 8 hrs)
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Respiratory Insufficiency
Keywords
critically ill patient, intensive care unit, mechanical ventilation, pandemic
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
The flow divider is connected to the ventilator. Half of the fresh gas flows to the patient, hallf to the artificial lung ( 1:1 ratio). For adequate ventilation tidal volume set on the ventilator is then doubled. Chosen respiratory and circulatory parameters are beeing noted.
Masking
None (Open Label)
Allocation
N/A
Enrollment
40 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
mechanically ventilated patients
Arm Type
Experimental
Arm Description
Adult ICU patients who are mechanically ventilated and who do not require complex modes of ventilation.
A designated flow divider (Ventil) will be used to divide inspiratory gas flow from ventilator in two separate streams - one to the patient and the second to the artificial lung
Intervention Type
Device
Intervention Name(s)
Ventil - a gas flow divider
Intervention Description
Checking ventilation parameters set and obtained and clinical parameters while ventilating the patient and an artificial lung simultaneously, using inspiratory flow divider.
Primary Outcome Measure Information:
Title
Number of cases in which it was necessary to stop using Ventil and to step- back to ventilation without this flow divider
Description
Ventil will be removed from the patient-ventilator circiuit in case of episodes of desaturation <90% (in pts without COPD) without reversibel reason; need for FiO2 increase by 10%; need for switch to other than CMV mode of ventillation need for neuromucular blockade or for deepen sedation because of assynchrony between patient and venilator cummulation of CO2>45 mm Hg (in pts without COPD) not responding to the increase of minute ventilation for 30 minutes; if Pplat >30 cmH2O; in case of new haemodynamic disturbances that cannot be explaned by other reasons; in case of increase or decrease of BP by 20%; increase or decrease of HR by 20%; in case of occurence of clinically important heart rhythm disturbances
Time Frame
48 hours
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
ICU patients who require mechanical ventilation
Exclusion Criteria:
Patients who require complex modes of ventilation will not be recruited
The sudy in an individual patient be discontinued if case of:
Respiratory Criteria:
episodes of desaturation <90% (in pts without COPD) without reversibel reason
need for FiO2 increase by 10%
need for switch to other than CMV mode of ventillation
need for neuromucular blockade or for deepen sedation because of assynchrony between patient and venilator
cummulation of CO2>45 mm Hg (in pts without COPD) not responding to the increase of minute ventilation for 30 minutes
Pplat >30 cmH2O
Circulatory criteria:
New haemodynamic disturbances that cannot be explaned by other reasons
↑ or ↓of BP by 20%
↑ or ↓of HR by 20%
clinically important heart rhythm disturbances
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Radoslaw Owczuk, prof
Phone
+48583493270
Email
r.owczuk@gumed.edu.pl
First Name & Middle Initial & Last Name or Official Title & Degree
Magdalena A Wujtewicz, dr
Phone
+48583493270
Email
magwuj@gumed.edu.pl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Radoslaw Owczuk, prof
Organizational Affiliation
Medical University of Gdansk
Official's Role
Principal Investigator
Facility Information:
Facility Name
Medical University of Gdansk
City
Gdansk
ZIP/Postal Code
80-214
Country
Poland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Magdalena A Wujtewicz
Phone
+48583493357
Email
magwuj@gumed.edu.pl
First Name & Middle Initial & Last Name & Degree
Radoslaw Owczuk
Phone
605408140
Email
r.owczuk@gumed.edu.pl
12. IPD Sharing Statement
Plan to Share IPD
Undecided
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Ventil Device Usefulness in Mechanically Ventilated ICU Patients
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