Neutrophil and Monocyte Deactivation Via the SeLective CytopheretIc Device - A Randomized Clinical Trial in Acute Kidney Injury
SeaStar Medical · NCT05758077
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · All sexes
- Healthy volunteers
- Not accepted (a condition is required)
- Study type
- Interventional · Not applicable
- Target enrollment
- 339
- US sites recruiting
- 24
- Study start
- April 17, 2023
- Record last updated
- October 22, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
This randomized, controlled, pivotal study is intended to determine whether up to ten sequential 24-hour treatments with the Selective Cytopheretic Device (SCD) will improve survival in patients with Acute Kidney Injury (AKI) requiring continuous kidney replacement therapy (CKRT) when compared to CKRT alone (standard of care). This study is further intended to determine whether SCD therapy will reduce the duration of maintenance dialysis secondary to AKI. This study will enroll approximately 339 subjects across 30 US sites. Participants will be patients in an intensive care unit (ICU) setting with a diagnosis of AKI requiring CKRT.
Being studied: Selective Cytopheretic Device; Standard of Care
Conditions: Acute Kidney Injury
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Admitted to an ICU requiring CKRT:
- Must have AKI stage 2 or greater at the time of CKRT initiation.
- Must have been on CKRT for at least 12 hours but no greater than 48 hours at the time of enrollment.
- At least 18 years of age but not older than 80 at the time of enrollment.
- One additional life-threatening organ dysfunction present.
- Acceptable vascular access for CKRT to include adequate lumen size and length of catheters.
- Initial (non-binding) commitment to maintaining current level of care for at least 96 hours.
- C-Reactive Protein >3.5 mg/dl.
Exclusion Criteria
- Not expected to survive next 24 hours.
- Anticipated transition to comfort measures or hospice in next 4 days.
- Terminal condition whereby the patient is not expected to survive 28 days or any condition in which therapy is regarded as futile by the PI.
- Advanced malignancy which is actively being treated or may be treated with palliative chemotherapy or radiation.
- ICU hospitalization > 14 days during this hospital admission (to include days spent at ICU of an outside hospital) at the time of screening.
- Active COVID-19 infection with a primary admission diagnosis of COVID-19.
- Chronic use of ventricular assist devices.
- ESRD requiring chronic kidney replacement therapy.
- History of CKD (greater than Stage 3).
- AKI stage 0 or stage 1 at the time of CKRT initiation.
- Non-ATN AKI diagnosis. We intend on relying on local nephrology subspecialty expertise to reasonably exclude non-ATN diagnoses based on clinical suspicions combined with prespecified objective criteria. If there is a reasonable suspicion that the subject has non-ATN AKI based on this, they will be excluded from the trial.
- Acute coronary syndromes, acute stroke, or acute major vascular compromise requiring medical or surgical interventions within 48 hours of randomization.
- Active hemorrhage requiring blood transfusions at the time of screening.
- Acute on Chronic Liver Failure.
- Suspicion of hepato-renal syndrome.
- Presence of any solid organ transplant at any time prior to admission.
- Severe burns with a modified Baux score > 100 (%TBSA+Age+17 for Inhalation Injury).
- Bone marrow transplant within the last year.
- Chronic immunosuppression with an average of >20 mg/day of prednisone or other steroid sparing immunosuppressants for the past 30 days prior to hospital admission.
- Individuals who have a history of primary or secondary immune disorders including, but not limited to, HIV or AIDS.
- Dry weight of >150kg.
- Platelet count \<15,000/mm3.
- Patient is a prisoner or member of a vulnerable population.
- Patient is pregnant or breast feeding.
- Concurrent enrollment in another interventional clinical trial for an investigational drug or device.
- Need for plasmapheresis.
Recruiting US locations
University of Alabama Birmingham Hospital
Birmingham, AL 35233
Ronald Reagan UCLA Medical Center
Los Angeles, CA 90095
Stanford University
Palo Alto, CA 94304
University of California San Francisco
San Francisco, CA 94143
AdventHealth Orlando
Orlando, FL 32803
Emory Healthcare
Atlanta, GA 30322
University of Iowa Hospital
Iowa City, IA 52242
Ochsner LSU Health Academic Medical Center
Shreveport, LA 71103
University of Maryland Medical Center
Baltimore, MD 21201
University of Michigan
Ann Arbor, MI 48109
Henry Ford Medical Center
Detroit, MI 48202
Mayo Clinic
Rochester, MN 55902
University of North Carolina
Chapel Hill, NC 27599
University of Cincinnati
Cincinnati, OH 45219
Cleveland Clinic
Cleveland, OH 44195
St Luke's University Hospital
Bethlehem, PA 19015
Saint Mary Medical Center
Langhorne, PA 19047
Medical University of South Carolina
Charleston, SC 29425
University of Texas Southwestern Medical Center
Dallas, TX 75390
Brooke Army Medical Center
Fort Sam Houston, TX 78234
Methodist Hospital Metropolitan
San Antonio, TX 78212
Methodist Hospital
San Antonio, TX 78229
University of Texas Health San Antonio
San Antonio, TX 78229
Sentara Health
Norfolk, VA 23507
Study contacts (from the official record)
- Mohamed Zidan, MD · 844-427-8100 · mzidan@seastarmed.com
- Kevin K Chung, MD · 844-427-8100 · kchung@seastarmed.com