RESCUE 1-19: Radiation Eliminates Storming Cytokines and Unchecked Edema as a 1-Day Treatment for COVID-19

Sponsor
Emory University (Other)
Overall Status
Terminated
CT.gov ID
NCT04366791
Collaborator
National Cancer Institute (NCI) (NIH)
47
2
1
22.5
23.5
1

Study Details

Study Description

Brief Summary

This phase I/II trial studies low-dose radiation therapy as a focal anti-inflammatory treatment for patients with pneumonia or SARS associated with COVID-19 infection.

Condition or Disease Intervention/Treatment Phase
  • Radiation: Low Dose Radiation Therapy
Phase 1/Phase 2

Detailed Description

PRIMARY OBJECTIVE:
  1. To compare treatment of COVID-19 between best supportive care plus provider's treatment choice versus best supportive care plus low-dose, whole-lung radiation therapy
OUTLINE:

Patients undergo 1 fraction of low-dose radiation therapy.

After completion of study treatment, patients are followed up at days 1-7, and 14 after last dose of intervention.

Study Design

Study Type:
Interventional
Actual Enrollment :
47 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
The RESCUE 1-19 Trial: Radiation Eliminates Storming Cytokines and Unchecked Edema as a 1-Day Treatment for COVID-19
Actual Study Start Date :
Apr 24, 2020
Actual Primary Completion Date :
Mar 11, 2022
Actual Study Completion Date :
Mar 11, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Supportive care (low-dose radiation therapy)

Patients undergo 1 fraction of low-dose radiation therapy.

Radiation: Low Dose Radiation Therapy
Undergo low-dose radiation therapy
Other Names:
  • Low Dose Radiation
  • Outcome Measures

    Primary Outcome Measures

    1. Rate of extubation (for intubated patients) [Screening up to 28 days after radiation therapy]

      The rate will be reported, along with a two-sided 95% exact binomial confidence interval, using the Clopper-Pearson method. The observed extubation rate will be compared to the null rate of 20% using a two-sided binomial test. Statistical significance is assessed at the 0.05 level.

    Secondary Outcome Measures

    1. Clinical outcome - Temperature [Screening up to 28 days after radiation therapy]

      Temperature in degrees (F)

    2. Clinical outcome - Heart Rate [Screening up to 28 days after radiation therapy]

      Heart rate in beats per minutes

    3. Clinical outcome - Systolic blood pressure [Screening up to 28 days after radiation therapy]

      Systolic blood pressure in mm Hg

    4. Clinical outcome - Oxygenation [Screening up to 28 days after radiation therapy]

      Oxygen saturation in percentage

    5. Clinical outcome - Respirations [Screening up to 28 days after radiation therapy]

      Respiratory rate in breaths per minute

    6. Clinical outcome - FiO2 [Screening up to 28 days after radiation therapy]

      FI02 in percentage

    7. Clinical outcome - PEEP [Screening up to 28 days after radiation therapy]

      Positive end expiratory pressure (PEEP) in cm H20

    8. Clinical outcome - Tidal volume [Screening up to 28 days after radiation therapy]

      Tidal volume in mL

    9. Clinical outcome - Intubation/Extubation events [Screening up to 28 days after radiation therapy]

      Extubation/intubation events in percentage

    10. Clinical outcome - Overall survival [Screening up to 28 days after radiation therapy]

      Survival in percentage

    11. Radiographic outcome - Chest xray [Screening up to 28 days after radiation therapy]

      Serial chest x-rays categorized using published scale into ordinal ranks 1-5 for SARS.

    12. Radiographic outcome - CT can [Screening up to 28 days after radiation therapy]

      CT scans with volume of consolidation measured in cubic centimeters.

    13. Serologic outcome - WBC [Screening up to 28 days after radiation therapy]

      White blood cell count in cell count x 10^3/mcL

    14. Serologic outcome - Hgb [Screening up to 28 days after radiation therapy]

      Hemoglobin in gm/dL

    15. Serologic outcome - Procalcitonin [Screening up to 28 days after radiation therapy]

      Procalcitonin in ng/mL

    16. Serologic outcome - ANC [Screening up to 28 days after radiation therapy]

      Absolute neutrophil count in cell count x 10^3/mcL

    17. Serologic outcome - Creatine kinase [Screening up to 28 days after radiation therapy]

      Creatine kinase in units/L

    18. Serologic outcome - Myoglobin [Screening up to 28 days after radiation therapy]

      Myoglobin in ng/mL

    19. Serologic outcome - Albumin [Screening up to 28 days after radiation therapy]

      Albumin in gm/dL

    20. Serologic outcome - PT/PTT [Screening up to 28 days after radiation therapy]

      Coagulation pathway time in seconds

    21. Serologic outcome - D-Dimer [Screening up to 28 days after radiation therapy]

      D-Dimer in ng/mL

    22. Serologic outcome - GGT [Screening up to 28 days after radiation therapy]

      Gamma-glutamyl transferase in units/L

    23. Serologic outcome -Triglycerides [Screening up to 28 days after radiation therapy]

      Trygliciericdes in mg/dL

    24. Serologic outcome -Ferritin [Screening up to 28 days after radiation therapy]

      Ferritin in ng/mL

    25. Serologic outcome -Fibrinogen [Screening up to 28 days after radiation therapy]

      Fibrinogen in mg/dL

    26. Serologic Immune markers flow cytometry [Screening up to 28 days after radiation therapy]

      Immune marker flow cytometry (refractive index)

    27. Serologic outcome -Bilirubin [Screening up to 28 days after radiation therapy]

      Bilirubin in mg/dL

    28. Serologic outcome - LDH [Screening up to 28 days after radiation therapy]

      Lactate Dehydrogenase in units/L

    29. Serologic outcome - Creatinine [Screening up to 28 days after radiation therapy]

      Creatinine in mg/dL

    30. Serologic outcome - EGFR [Screening up to 28 days after radiation therapy]

      Estimated Glomerular Filtration Rate in mL/min/m2

    31. Serologic outcome - CRP [Screening up to 28 days after radiation therapy]

      C-Reactive Protein in mg/L

    32. Serologic outcome - ALT [Screening up to 28 days after radiation therapy]

      Alanine Aminotransferase in units/L

    33. Serologic outcome - AST [Screening up to 28 days after radiation therapy]

      Asparatate Aminotransferase in units/L

    34. Serologic outcome - Troponin-I [Screening up to 28 days after radiation therapy]

      Troponin-I in ng/mL

    35. Serologic outcome - BNP [Screening up to 28 days after radiation therapy]

      B-Natriuretic Peptid in pg/mL

    36. Serologic outcome - Blood Gases pH [Screening up to 28 days after radiation therapy]

      pH (no unit)

    37. Serologic outcome - Blood Gases pO2 [Screening up to 28 days after radiation therapy]

      pressure of O2 in mm Hg

    38. Serologic outcome - Blood Gases pCO2 [Screening up to 28 days after radiation therapy]

      pressure of CO2 in mm Hg

    39. Serologic outcome - Lactic Acid [Screening up to 28 days after radiation therapy]

      Lactic Acid in mmol/L

    40. Serologic outcome - IL-6 [Screening up to 28 days after radiation therapy]

      Interleukin-6 in pg/mL

    41. Serologic outcome - Potassium [Screening up to 28 days after radiation therapy]

      Potassium in mmol/L

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Have had a positive test confirming the diagnosis of COVID-19

    • Have had clinical signs of severe acute respiratory syndrome or pneumonia (dyspnea, cough, with need for oxygen support at the time of enrollment)

    • Have visible consolidations/ground glass opacities on chest x-ray or computed tomography

    • Have received pre-intubation respiratory support or undergone endotracheal intubation and have been on ventilator support for no longer than 5 (five) calendar days prior to the schedule date of delivery of low-dose radiation therapy.

    • Willingness and ability of the subject to comply with scheduled visits, protocol-specified laboratory tests, other study procedures, and study restrictions

    • Evidence of a signed informed consent/assent indicating that the subject is aware of the infectious nature of the disease and has been informed of the procedures to be followed, potential risks and discomforts, potential benefits, and other pertinent aspects of study participation

    Exclusion Criteria:
    • No use of disallowed medications 1 day prior to delivery of LDRT: Azithromycin, chloroquine, hydrochloroquine, COVID-targeted antiviral medications

    • Pregnant and/or planned to be pregnant within in next 6 months

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Emory University Hospital Midtown/Winship Cancer Institute Atlanta Georgia United States 30308
    2 Emory Saint Joseph's Hosptial Atlanta Georgia United States 30342

    Sponsors and Collaborators

    • Emory University
    • National Cancer Institute (NCI)

    Investigators

    • Principal Investigator: Mohammad Khan, MD, PhD, Emory University Hospital/Winship Cancer Institute

    Study Documents (Full-Text)

    More Information

    Publications

    None provided.
    Responsible Party:
    Mohammad K. Khan, Study Principal Investigator, Emory University
    ClinicalTrials.gov Identifier:
    NCT04366791
    Other Study ID Numbers:
    • STUDY00000476
    • NCI-2020-02676
    • RAD5002-20
    • P30CA138292
    First Posted:
    Apr 29, 2020
    Last Update Posted:
    Mar 29, 2022
    Last Verified:
    Mar 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    Yes
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 29, 2022