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OpenTrials
Completed

NCT Number: NCT04395911

Safety and Efficacy of SCD in AKI or ARDS Patients Associated With COVID-19 Infections

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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Key information

Conditions

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Kentucky, Lexington, Kentucky, United States

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Informed consent obtained
  • Positive COVID-19 test
  • Must be receiving medical care in an intensive care nursing situation
  • Non-pregnant females
  • Intent to deliver full supportive care through aggressive management utilizing all available therapies for a minimum of 96 hours.
  • Platelet count >30,000/mm3 at Screening
  • Clinical diagnosis of AKI requiring CRRT or ARDS

Exclusion criteria

  • Cardiovascular instability that precludes initiation of continuous renal replacement therapy (CRRT).
  • Irreversible brain damage based on available historical and clinical information.
  • Presence of any solid organ transplant at any time.
  • Patients with stem cell transplant in the previous 100 days or who have not engrafted.
  • Acute or chronic use of circulatory support device other than ECMO such as LVADs, RVADs, BIVADs.
  • Metastatic malignancy which is actively being treated or may be treated with chemotherapy or radiation during the subsequent three month period after study treatment.
  • Chronic immunosuppression defined as >20 mg prednisone qd alone without other immunosuppressant medications (ie (cyclophosphamide, azathioprine, methotrexate, rituximab, mycophenolate, cyclosporine).
  • Patient is moribund or chronically debilitated for whom full supportive care is not indicated.
  • Concurrent enrollment in another interventional clinical trial. Patients enrolled in observational studies (NO TEST DEVICE OR DRUG USED) are allowed to participate.
  • Any reason the Investigator deems exclusionary.

Treatment and study plan

SCD

Device

cytopheretic device

Primary outcomes

  1. Mortality at Day 60

    Time frame: 60 days post treatment

    All cause mortality at Day 60

  2. Dialysis Dependency

    Time frame: 60 days post treatment

    Dialysis Dependency at Day 60

  3. Ventilation at Day 28

    Time frame: 28 days post treatment

    Ventilation free survival at Day 28

Secondary outcomes

  1. Dialysis Dependency

    Time frame: 28 days post treatment

    Dialysis Dependency at Day 28

  2. Mortality at Day 28

    Time frame: 28 days post treatment

    All cause mortality at Day 28

  3. Urinary output change

    Time frame: 10 days of treatment

    Change from baseline in urine output

  4. P02/FiO2 change

    Time frame: 10 days of treatment

    Change from baseline in PO2/FiO2

  5. Safety Assessments

    Time frame: 10 days of treatment

    Assessment of SAEs, AE and UADEs

  6. SCD Integrity

    Time frame: 10 days of treatment

    Assessment of device performance

Sponsors and collaborators

Lead sponsor

SeaStar Medical

Industry

Registry information

Official study title

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

Important dates

Study start
2020
Primary completion
2021
Study completion
2021
First posted
May 20, 2020
Registry last updated
Aug 5, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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