Bleeding is a significant complication in cardiac surgery, with 10-15% of open cardiac surgery patients experiencing major intra- or post-operative bleeding. To address this unmet need, PLAS-FREE LTD has developed ClearPlasma™, a single-use, extracorporeal plasma filtration device which extracts plasminogen from plasma to reduce fibrinolysis. The resulting plasminogen-depleted plasma (PDP) is expected to reduce risk of fibrinolysis and bleeding in patients undergoing plasma transfusions.
Bleeding is a significant complication in cardiac surgery, with 10-15% of open cardiac surgery patients experiencing major intra- or post-operative bleeding. Bleeding complications are associated with worse clinical outcomes, including a higher risk of infection, ischemic events attributable to hypo-perfusion (e.g., myocardial infarction, acute kidney injury), in-hospital mortality, and transfusion-related adverse events. Additionally, bleeding complications are an important driver of blood product utilization in cardiac surgery. Coagulopathy and bleeding after cardiac surgery are often a multifactorial problem, thus there is unmet need to find new technologies that can give better care to these bleeding patients. In 2016, it was estimated that one million people throughout the world undergo cardiac surgery each year. Most of these surgeries are Coronary artery bypass grafting and valves replacement. Coronary artery bypass grafting (CABG) is still the most commonly performed cardiac surgery procedure worldwide, representing annual volumes of approximately 200,000 isolated cases in the US and an average incidence rate of 62 per 100,000 inhabitants in western European countries. Aortic valve replacement is procedure that treat diseases affecting the aortic valve, one of four valves that control blood flow through the heart. In the United States, it is estimated that 2.5% of the general population, 8.5% of those 65-74 years of age and 13.2% of those ≥75 years of age have moderate to severe valvular diseases. These surgeries are commonly done in the western countries, however, the ability to halt the bleed remain challenge for most clinicians. Failed or delayed treatment of a massive bleeding can result in irreversible end-organ damage (e.g., renal failure), cardiovascular events (e.g., stroke, myocardial injury) or death, accompanied by significantly increased costs. Fibrin clot breakdown is actively mediated by plasmin, a serine protease which cleaves fibrin. Administration of plasma depleted of plasminogen, the precursor of plasmin, may shift the balance towards coagulation. PLAS-FREE LTD has developed ClearPlasma™, a single-use, extracorporeal plasma filtration device which extracts plasminogen from plasma to reduce fibrinolysis. The resulting plasminogen-depleted plasma (PDP) is expected to reduce risk of fibrinolysis and bleeding in patients undergoing plasma transfusions.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
130
ClearPlasma ClearPlasma™ is an extra-corporeal plasma filtration device, designed to specifically extract plasminogen, a protein that drives fibrinolysis, from up to 250 mL of plasma. ClearPlasma™ is a non-pyrogenic, sterile, single-use medical device
Charles University Teaching Hospital
Hradec Králové, Czechia
University Hospital Olomouc
Olomouc, Czechia
University Hospital Ostrava
Ostrava, Czechia
Wolfson Medical center
Holon, Israel
Rabin Medical Center - Beilinson
Petah Tikva, Israel
Sheba Medical Center
Ramat Gan, Israel
Szpital Kliniczny im. Heliodora Święcickiego Uniwersytetu Medycznego w Poznaniu
Poznan, Poland
Narodowy Instytut Kardiologii Stefana kardynała Wyszyńskiego Państwowy Instytut Badawczy
Warsaw, Poland
ClearPlasma efficacy
Post-operative blood loss (mL) within 24 hours after surgery, defined as total output of mediastinal and pleural chest tubes. \[time frame: up to 24 hours after procedure\]
Time frame: 30 days
Transfusion- related SAE
Comparison of the number of transfusion- related SAEs between the groups. \[time frame: discharge\]obtained through filtration with ClearPlasma™ in patients after coronary artery bypass grafting or valve replacement surgery and to compare it to the same procedure carried out using FFP units.
Time frame: 30 days
Hemoglobin levels
Comparison of hemoglobin levels drop between the groups \[time frame: measured at patient's departure from the operating room/admitting to the ICU and compared to the lowest hemoglobin value until discharge\]
Time frame: 30 days
Post-operative blood loss
Post-operative blood loss (mL) within 12 hours after surgery, defined as total output of mediastinal and pleural chest tubes. \[time frame: up to 12 hours after procedure\]
Time frame: 30 days
Total blood loss
Total blood loss, defined as total output of chest tubes from insertion till removal \[time frame: drain removal\]
Time frame: 30 days
ClearPlasma
Ratio of bleeding events between the groups \[time frame: discharge\]
Time frame: 30 days
bleeding events-
Ratio of bleeding events requiring re-intervention up to discharge \[time frame: discharge\]
Time frame: 30 days
major bleeding
Ratio of major bleeding defined as blood loss greater than \>1000 mL in first 12 h and/or need for surgical revision owing to bleeding; \[time frame: discharge\]
Time frame: 30 days
Mortality
All-cause mortality\[time frame: 30 days\]
Time frame: 30 days
In- hospital mortality
In- hospital mortality \[time frame: discharge\]
Time frame: 30 days
Number of blood units transfused
The number of units of allogeneic blood products transfused until discharge \[time frame: discharge\]: 1. Red blood cells (RBC) units transfused; 2. Plasma (PDP/FFP) units transfused; 3. Platelet concentrates units transfused
Time frame: 30 days
Length of stay in the ICU
Length of stay in the ICU \[Time Frame: discharge\]
Time frame: 30 days
Hospitalization Duration
Total length of hospitalization \[Time Frame: discharge\]
Time frame: 30 days
Incidence of ischemic outcomes
Comparison of the incidence of ischemic outcomes defined as a composite of stroke, transient ischemic attack, acute myocardial infarction, PE and/or acute renal failure \[time frame: discharge\] Study Groups
Time frame: 30 days
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