Flow-flow ECCO2-R and 4 ml/kg Tidal Volume vs. 6 ml/kg Tidal Volume to Enhance Protection From VILI in Acute Lung Injury (ELP)
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT01522599|
Recruitment Status : Terminated (Financial hardship)
First Posted : January 31, 2012
Last Update Posted : June 17, 2014
|Condition or disease||Intervention/treatment||Phase|
|Acute Respiratory Distress Syndrome||Other: ARDS-Net Strategy Other: ECCO2-R||Phase 3|
The trial will test the hypothesis that a VT of 4 ml/kg PBW combined with low flow CO2 removal improves outcome in patients with severe ARDS (PFs ≤ 200 and PEEP ≥ 10) compared to ventilation with a VT of 6 ml/kg PBW. The study will accrue a maximum of 230 patients over approximately 12-18 months.
PRIMARY END-POINT: Number of ventilator-free days (VFDs) during the 28 days immediately after randomization
SECONDARY END-POINTS: 28 and 90-day all-cause mortality; number of ICU-free days during the 28 days immediately after randomization; cumulative incidence of: first episode of refractory hypoxemia (during 28 days after randomization), use of rescue therapies, first day that meet criteria for weaning, SOFA-free and severe adverse events.
Patients in CONTROL will be treated according to a modified, simplified version of The ARDS-Network lung protective lower tidal volume. Patients in TREATMENT group will be treated according to the ARDS-Net protocol modified (VT reduced by 1 ml/kg PBW at intervals ≤ 2 hours until VT = 4ml/kg PBW and the use of low-flow CO2 removal with a Plateau Pressure Goal: ≤ 25 cm H2O).
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||230 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Official Title:||Flow-flow ECCO2-R and 4 ml/kg Tidal Volume vs. 6 ml/kg Tidal Volume to Enhance Protection From Ventilator Induced Lung Injury in Acute Lung Injury (ELP)|
|Study Start Date :||April 2012|
|Actual Primary Completion Date :||January 2014|
|Actual Study Completion Date :||January 2014|
|Active Comparator: ARDS-Net strategy (Control)||
Other: ARDS-Net Strategy
Treatment according to the ARDS-Net protocol (The Acute Respiratory Distress Syndrome Network N Engl J Med 2000; 342:1301-1308May 4, 2000)
Other Name: Protective ventilation
|Experimental: ECCO2-R with 4 mL/Kg Vt (Treatment)||
Ventilation with Tidal Volume of 4 ml/kg PBW and low flow CO2 removal
Other Name: Further protective ventilation
- Number of ventilator-free days during the 28 days immediately after randomization [ Time Frame: 28 DAYS ]VFDs is a composite endpoint. VFD to day 28 is defined as the number of days after initiating unassisted breathing to day 28 after randomization, assuming a patient survives for at least two consecutive calendar days after initiating nassisted breathing and remains free of assisted breathing. If a patient dies prior to day 28 or is still receiving assisted breathing at day 27, his/her VFDs will be zero.
- 28-day all-cause mortality [ Time Frame: 28 days ]All patients will be classified as either "alive at Study Day 28" or, if dead, "dead at Study Day 28." For example, day zero is the day of randomization and day 1 is the next day and encompasses all events that occur midnight-to-midnight, etc.
- 90-day all-cause mortality. [ Time Frame: 90 days ]All patients will be classified as either "alive at Study Day 90" or, if dead, "dead at Study Day 90. Patients alive in hospital or in any health care facility at day 90 will be considered to have survived.
- Number of ICU-free days during the 28 days immediately after randomization (ICU-FD). [ Time Frame: 28 days ]ICU-FDs are defined as the number of days from the time of ICU discharge to day 28 after randomization, assuming survival for at least two consecutive calendar days after ICU discharge and continued stay outside the ICU setting to day 28. If a patient returns to the ICU and subsequently needs ICU admission to day 28, ICU-FDs will be counted from the end of the last period of ICU discharge to day 28.
- Cumulative incidence of first episode of refractory hypoxemia (during 28 days after randomization). [ Time Frame: 28 days ]Refractory hypoxemia is defined as PaO2 < 60 mm Hg for at least 1 hour while receiving an FIO2 of 1.0
- Cumulative incidence of the use of rescue therapies. [ Time Frame: 28 days ]The first day inhaled nitric oxide or prone position or high-frequency oscillation or high-frequency oscillatory ventilation or extracorporeal membrane oxygenation or any combinations of these therapies will be tabulated.
- Cumulative incidence of first day that meet criteria for weaning readiness during 28 days after randomization. [ Time Frame: 28 days ]
Weaning readiness will be defined if the following 4 criteria are met for the last 30 minutes during a spontaneous breathing trial (SBT).
- SpO2 ≥ 90% and / or PaO2 ≥ 60 mm Hg; PaO2 to take precedence if both available
- Respiratory Rate ≤ 35 / min
- pH ≥ 7.30
- No respiratory distress
- Cumulative SOFA-free score between randomization and day 28. [ Time Frame: 28 days ]The SOFA-free score is calculated as the maximum daily score, minus the observed SOFA score. To monitor the degree of variation of the patient's SOFA score (as improvement or worsening) the daily difference between the maximum score and the observed score will be summed up for each day between randomization and day 28. Patients dying before the 28th day cannot continue to increase their cumulative SOFA-free score. In this way, the larger the cumulative score reached, the higher is the improvement of the patient and the probability of being alive at day 28.
- Cumulative incidence of severe adverse events during 28 days after randomization. [ Time Frame: 28 days ]Adverse events that are considered to be related to ECCO2-R and that follows a reasonable temporal sequence from the ECCO2-R and that could readily have been produced by ECCO2-R will be classified as: "DEVICE RELATED" or "PATIENT RELATED"
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01522599
|University of Turin - Department of Anesthesia and Intensive Care Medicine|
|Turin, Italy, 10126|
|Principal Investigator:||Vito Marco VM Ranieri, MD||Department of Anesthesia and Intensive Care Medicine, University of Turin, Italy|
|Study Chair:||Antonio A Pesenti, MD||Department of Perioperative Medicine and Intensive Care, San Gerardo Hospital, Monza, Italy|