Clinical Trials Logo

Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT04366791
Other study ID # STUDY00000476
Secondary ID NCI-2020-02676RA
Status Terminated
Phase Phase 1/Phase 2
First received
Last updated
Start date April 24, 2020
Est. completion date March 11, 2022

Study information

Verified date March 2022
Source Emory University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Description:

PRIMARY OBJECTIVE: I. 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.


Recruitment information / eligibility

Status Terminated
Enrollment 47
Est. completion date March 11, 2022
Est. primary completion date March 11, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Radiation:
Low Dose Radiation Therapy
Undergo low-dose radiation therapy

Locations

Country Name City State
United States Emory Saint Joseph's Hosptial Atlanta Georgia
United States Emory University Hospital Midtown/Winship Cancer Institute Atlanta Georgia

Sponsors (2)

Lead Sponsor Collaborator
Emory University National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Rate of extubation (for intubated patients) 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. Screening up to 28 days after radiation therapy
Secondary Clinical outcome - Temperature Temperature in degrees (F) Screening up to 28 days after radiation therapy
Secondary Clinical outcome - Heart Rate Heart rate in beats per minutes Screening up to 28 days after radiation therapy
Secondary Clinical outcome - Systolic blood pressure Systolic blood pressure in mm Hg Screening up to 28 days after radiation therapy
Secondary Clinical outcome - Oxygenation Oxygen saturation in percentage Screening up to 28 days after radiation therapy
Secondary Clinical outcome - Respirations Respiratory rate in breaths per minute Screening up to 28 days after radiation therapy
Secondary Clinical outcome - FiO2 FI02 in percentage Screening up to 28 days after radiation therapy
Secondary Clinical outcome - PEEP Positive end expiratory pressure (PEEP) in cm H20 Screening up to 28 days after radiation therapy
Secondary Clinical outcome - Tidal volume Tidal volume in mL Screening up to 28 days after radiation therapy
Secondary Clinical outcome - Intubation/Extubation events Extubation/intubation events in percentage Screening up to 28 days after radiation therapy
Secondary Clinical outcome - Overall survival Survival in percentage Screening up to 28 days after radiation therapy
Secondary Radiographic outcome - Chest xray Serial chest x-rays categorized using published scale into ordinal ranks 1-5 for SARS. Screening up to 28 days after radiation therapy
Secondary Radiographic outcome - CT can CT scans with volume of consolidation measured in cubic centimeters. Screening up to 28 days after radiation therapy
Secondary Serologic outcome - WBC White blood cell count in cell count x 10^3/mcL Screening up to 28 days after radiation therapy
Secondary Serologic outcome - Hgb Hemoglobin in gm/dL Screening up to 28 days after radiation therapy
Secondary Serologic outcome - Procalcitonin Procalcitonin in ng/mL Screening up to 28 days after radiation therapy
Secondary Serologic outcome - ANC Absolute neutrophil count in cell count x 10^3/mcL Screening up to 28 days after radiation therapy
Secondary Serologic outcome - Creatine kinase Creatine kinase in units/L Screening up to 28 days after radiation therapy
Secondary Serologic outcome - Myoglobin Myoglobin in ng/mL Screening up to 28 days after radiation therapy
Secondary Serologic outcome - Albumin Albumin in gm/dL Screening up to 28 days after radiation therapy
Secondary Serologic outcome - PT/PTT Coagulation pathway time in seconds Screening up to 28 days after radiation therapy
Secondary Serologic outcome - D-Dimer D-Dimer in ng/mL Screening up to 28 days after radiation therapy
Secondary Serologic outcome - GGT Gamma-glutamyl transferase in units/L Screening up to 28 days after radiation therapy
Secondary Serologic outcome -Triglycerides Trygliciericdes in mg/dL Screening up to 28 days after radiation therapy
Secondary Serologic outcome -Ferritin Ferritin in ng/mL Screening up to 28 days after radiation therapy
Secondary Serologic outcome -Fibrinogen Fibrinogen in mg/dL Screening up to 28 days after radiation therapy
Secondary Serologic Immune markers flow cytometry Immune marker flow cytometry (refractive index) Screening up to 28 days after radiation therapy
Secondary Serologic outcome -Bilirubin Bilirubin in mg/dL Screening up to 28 days after radiation therapy
Secondary Serologic outcome - LDH Lactate Dehydrogenase in units/L Screening up to 28 days after radiation therapy
Secondary Serologic outcome - Creatinine Creatinine in mg/dL Screening up to 28 days after radiation therapy
Secondary Serologic outcome - EGFR Estimated Glomerular Filtration Rate in mL/min/m2 Screening up to 28 days after radiation therapy
Secondary Serologic outcome - CRP C-Reactive Protein in mg/L Screening up to 28 days after radiation therapy
Secondary Serologic outcome - ALT Alanine Aminotransferase in units/L Screening up to 28 days after radiation therapy
Secondary Serologic outcome - AST Asparatate Aminotransferase in units/L Screening up to 28 days after radiation therapy
Secondary Serologic outcome - Troponin-I Troponin-I in ng/mL Screening up to 28 days after radiation therapy
Secondary Serologic outcome - BNP B-Natriuretic Peptid in pg/mL Screening up to 28 days after radiation therapy
Secondary Serologic outcome - Blood Gases pH pH (no unit) Screening up to 28 days after radiation therapy
Secondary Serologic outcome - Blood Gases pO2 pressure of O2 in mm Hg Screening up to 28 days after radiation therapy
Secondary Serologic outcome - Blood Gases pCO2 pressure of CO2 in mm Hg Screening up to 28 days after radiation therapy
Secondary Serologic outcome - Lactic Acid Lactic Acid in mmol/L Screening up to 28 days after radiation therapy
Secondary Serologic outcome - IL-6 Interleukin-6 in pg/mL Screening up to 28 days after radiation therapy
Secondary Serologic outcome - Potassium Potassium in mmol/L Screening up to 28 days after radiation therapy
See also
  Status Clinical Trial Phase
Active, not recruiting NCT04244474 - Effect of Vitamin D Supplementation on Improvement of Pneumonic Children Phase 1/Phase 2
Completed NCT05815264 - Clinical Trial of 23-valent Pneumococcal Polysaccharide Vaccine in Healthy Chinese Population Aged 2 Years and Above Phase 1
Recruiting NCT04589936 - Prone Position to Improve Oxygenation in COVID-19 Patients Outside Critical Care N/A
Completed NCT02905383 - The Effect of Exercise on Physical Function and Health in Older People After Discharge From Hospital N/A
Completed NCT06210737 - A Study to Evaluate Persistence of Immunity of PCV13 in Healthy Population Aged 2 Months,7 Months-5 Years Phase 4
Terminated NCT03944551 - Bubble Continuous Positive Airway Pressure for Children With Severe Pneumonia in Mali, Africa N/A
Terminated NCT04660084 - Impact of Molecular Testing on Improved Diagnosis, Treatment and Management of CAP N/A
Not yet recruiting NCT05649891 - Checklists Resuscitation Emergency Department N/A
Withdrawn NCT05702788 - Efficacy and Safety of Jaktinib in Participants With Severe Novel Coronavirus Pneumonia(COVID-19) Phase 2
Not yet recruiting NCT04171674 - Pharmacokinetics of High-dose Ceftobiprole in Community-acquired Pneumonia Under Mechanical Ventilation. N/A
Active, not recruiting NCT03140163 - Screening for Pneumonia: A Comparison of Ultra Low Dose Chest CT [ULD-CT] and Conventional Chest Radiography [CXR] N/A
Completed NCT02864420 - Hospitalization at Home: The Acute Care Home Hospital Program for Adults N/A
Completed NCT02638649 - Prehospital Use of Ultrasound in Undifferentiated Shortness of Breath
Recruiting NCT02515565 - Physiotherapy in Patients Hospitalized Due to Pneumonia. N/A
Completed NCT02105298 - Effect of Volume and Type of Fluid on Postoperative Incidence of Respiratory Complications and Outcome (CRC-Study) N/A
Completed NCT01416519 - Physiotherapy Technique Decreases Respiratory Complications After Cardiac Operation N/A
Completed NCT01446926 - Study of Investigational Pneumococcal Vaccine in Healthy Adults, Toddlers and Infants Phase 1
Completed NCT01399723 - Amoxicillin Versus Benzyl Penicillin for Treatment of Children Hospitalised With Severe Pneumonia Phase 3
Terminated NCT02358642 - Drug to Prevent Pneumonia in the Tube Fed Phase 4
Completed NCT01416506 - Community-Acquired Pneumonia (CAP) Surveillance N/A