ART-2 Pilot - Driving Pressure Limited Ventilation for Patients With ARDS (ART2pilot)
Primary Purpose
Acute Respiratory Distress Syndrome
Status
Completed
Phase
Phase 1
Locations
Study Type
Interventional
Intervention
Driving pressure limited ventilation
Conventional ventilation
Sponsored by
About this trial
This is an interventional treatment trial for Acute Respiratory Distress Syndrome
Eligibility Criteria
Inclusion criteria:
- Patients on invasive mechanical ventilation with diagnosis of ARDS of less than 72 hours duration.
Exclusion criteria:
- Less than 18 years old.
- Presence of any contraindication to hypercapnia as suspected or confirmed intracranial hypertension or recent (<7 days) acute coronary syndrome.
- Patients in which a high probability of death within 24 hours is anticipated.
- Patients under exclusive palliative care.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Driving pressure limited ventilation
Conventional ventilation
Arm Description
Driving pressure limited ventilation
Mechanical ventilation as proposed in the ARDSNet protocol.
Outcomes
Primary Outcome Measures
Mean driving pressure between day 1 and day 3
Driving pressure is the difference between plateau pressure and PEEP. It will be measured every morning in patients without spontaneous efforts. As every patients will have up to three measurements, we will consider the mean driving pressure for each patient.
Secondary Outcome Measures
Adherence to study procedures: daily adjustement of driving pressure in experimental group and tidal volume in the control group
Rate of driving pressure equal or lower than 13cmH2O
Mean PEEP from day 1 to 7
Mean tidal volume from day 1 to day 7
Mean static compliance of the respiratory system from day 1 to day 7
Mean plateau pressure from day 1 to day 7
Mean driving pressure from day 1 to day 7
Mean respiratory rate from day 1 to day 7
Barotrauma
Severe acidosis (pH <7.1)
Other adverse events
Length of stay in intensive care unit
Length of stay in hospital
Mechanical ventilation free days from day 0 to day 28
ICU mortality
In-hospital mortality
28-day survival
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT02365038
Brief Title
ART-2 Pilot - Driving Pressure Limited Ventilation for Patients With ARDS
Acronym
ART2pilot
Official Title
ART-2 Pilot: A Controlled, Randomized Trial to Assess the Feasiblity of a Driving Pressure Limited Ventilation vs. Standard Strategy (ARDSNet) in Patients With ARDS
Study Type
Interventional
2. Study Status
Record Verification Date
February 2015
Overall Recruitment Status
Completed
Study Start Date
June 12, 2015 (Actual)
Primary Completion Date
February 25, 2017 (Actual)
Study Completion Date
July 1, 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospital do Coracao
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This is a multicenter randomized controlled pilot trial to investigate the feasibility of a driving pressure limited mechanical ventilation strategy compared to the ARDS Clinical Network strategy (conventional strategy) in patients with acute respiratory distress syndrome (ARDS).
Detailed Description
Mechanical ventilation has the potential to produce or worsen alveolar injury. Driving pressure is the difference between plateau pressure and PEEP. Evidence from observational studies suggests that elevated driving pressure is the main independent determinant of ventilator-induced lung injury, however clinical trials are needed to establish whether targeting low driving pressures can improve clinical outcomes in patients with acute respiratory distress syndrome (ARDS). Thus, ART2pilot is a multicenter randomized controlled trial to assess the feasibility of a driving pressure limited mechanical ventilation strategy compared to the ARDS Clinical Network strategy (conventional strategy) in patients with ARDS. Patients considered to this trial are those in mechanical ventilation with diagnosis of ARDS of less than 72 hours duration. We will exclude patients with less than 18 years old; contraindication to hypercapnia such as intracranial hypertension or recent acute coronary syndrome; patients in which a high probability of death within 24 hours is anticipated and patients under exclusive palliative care. Eligible patients will be randomized to the driving pressure limited ventilation strategy or ARDSNet strategy. The primary outcome is driving pressure between days 1 and 3.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Respiratory Distress Syndrome
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
20 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Driving pressure limited ventilation
Arm Type
Experimental
Arm Description
Driving pressure limited ventilation
Arm Title
Conventional ventilation
Arm Type
Active Comparator
Arm Description
Mechanical ventilation as proposed in the ARDSNet protocol.
Intervention Type
Other
Intervention Name(s)
Driving pressure limited ventilation
Intervention Description
We will use volume controlled ventilation or pressure support in the weaning phase. We will adjust tidal volume between 3 and 8 mL/Kg of predicted body weight in order to achieve a driving pressure of 13 cmH2O. The respiratory rate will be titrated to achieve a pH between 7.30 and 7.45 (maximum respiratory rate is 50 breathings per minute). We will not limit plateau pressure in this arm.
Intervention Type
Other
Intervention Name(s)
Conventional ventilation
Other Intervention Name(s)
ARDSNet strategy
Intervention Description
ARDSNet Strategy: conventional mechanical ventilation strategy with tidal volume between 4 and 6 mL/kg of predicted body weight and plateau pressure limited to 30 cmH2O.
Primary Outcome Measure Information:
Title
Mean driving pressure between day 1 and day 3
Description
Driving pressure is the difference between plateau pressure and PEEP. It will be measured every morning in patients without spontaneous efforts. As every patients will have up to three measurements, we will consider the mean driving pressure for each patient.
Time Frame
Day 1 to Day 3 after randomization
Secondary Outcome Measure Information:
Title
Adherence to study procedures: daily adjustement of driving pressure in experimental group and tidal volume in the control group
Time Frame
Days 1 to 7
Title
Rate of driving pressure equal or lower than 13cmH2O
Time Frame
Days 1 to 3 after randomization
Title
Mean PEEP from day 1 to 7
Time Frame
Days 1 to 7
Title
Mean tidal volume from day 1 to day 7
Time Frame
Days 1 to 7
Title
Mean static compliance of the respiratory system from day 1 to day 7
Time Frame
Days 1 to 7
Title
Mean plateau pressure from day 1 to day 7
Time Frame
Days 1 to 7
Title
Mean driving pressure from day 1 to day 7
Time Frame
Days 1 to 7
Title
Mean respiratory rate from day 1 to day 7
Time Frame
Days 1 to 7
Title
Barotrauma
Time Frame
Days 1 to 7
Title
Severe acidosis (pH <7.1)
Time Frame
Days 1 to 7
Title
Other adverse events
Time Frame
Days 1 to 7
Title
Length of stay in intensive care unit
Time Frame
ICU stay
Title
Length of stay in hospital
Time Frame
In-hospital stay
Title
Mechanical ventilation free days from day 0 to day 28
Time Frame
From day 0 to day 28
Title
ICU mortality
Time Frame
ICU stay
Title
In-hospital mortality
Time Frame
Hospital stay
Title
28-day survival
Time Frame
From day 0 to day 28
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria:
Patients on invasive mechanical ventilation with diagnosis of ARDS of less than 72 hours duration.
Exclusion criteria:
Less than 18 years old.
Presence of any contraindication to hypercapnia as suspected or confirmed intracranial hypertension or recent (<7 days) acute coronary syndrome.
Patients in which a high probability of death within 24 hours is anticipated.
Patients under exclusive palliative care.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alexandre B Cavalcanti, MD, PhD
Organizational Affiliation
Hospital do Coracao (Heart Hospital)
Official's Role
Study Chair
12. IPD Sharing Statement
Citations:
PubMed Identifier
32069068
Citation
Pereira Romano ML, Maia IS, Laranjeira LN, Damiani LP, Paisani DM, Borges MC, Dantas BG, Caser EB, Victorino JA, Filho WO, Amato MBP, Cavalcanti AB. Driving Pressure-limited Strategy for Patients with Acute Respiratory Distress Syndrome. A Pilot Randomized Clinical Trial. Ann Am Thorac Soc. 2020 May;17(5):596-604. doi: 10.1513/AnnalsATS.201907-506OC.
Results Reference
derived
Learn more about this trial
ART-2 Pilot - Driving Pressure Limited Ventilation for Patients With ARDS
We'll reach out to this number within 24 hrs