SCD
Devicecytopheretic device
NCT Number: NCT04395911
Selective Cytopheretic Device (SCD) treatments will improve survival in patients testing positive for COVID-19 infection diagnosed with Acute Kidney Injury (AKI) or ARDS.
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Inclusion criteria
Exclusion criteria
cytopheretic device
Time frame: 60 days post treatment
All cause mortality at Day 60
Time frame: 60 days post treatment
Dialysis Dependency at Day 60
Time frame: 28 days post treatment
Ventilation free survival at Day 28
Time frame: 28 days post treatment
Dialysis Dependency at Day 28
Time frame: 28 days post treatment
All cause mortality at Day 28
Time frame: 10 days of treatment
Change from baseline in urine output
Time frame: 10 days of treatment
Change from baseline in PO2/FiO2
Time frame: 10 days of treatment
Assessment of SAEs, AE and UADEs
Time frame: 10 days of treatment
Assessment of device performance
SeaStar Medical
Industry
A Multi-Center Pilot Study to Assess the Safety and Efficacy of a Selective Cytopheretic Device (SCD) in Patients Developing Acute Kidney Injury (AKI) or Acute Respiratory Distress Syndrome (ARDS) Associated With COVID-19 Infection
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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