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Hydroxychloroquine in SARS-CoV-2 (COVID-19) Pneumonia Trial

Primary Purpose

SARS-CoV-2 Pneumonia, COVID-19

Status
Withdrawn
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Hydroxychloroquine
Sponsored by
Kootenai Health
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for SARS-CoV-2 Pneumonia focused on measuring SARS-CoV-2, Pneumonia, Hydroxychloroquine, COVID-19

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Age > 18 years of age
  2. SARS-CoV-2 positive per FDA approved RT-PCR (reverse transcription-polymerase chain reaction)
  3. Acute hypoxia (O2 sat < 90 % or paO2 < 60 on room air), or above baseline chronic O2 requirement
  4. Inpatient admission

Exclusion Criteria:

  1. Requires supplemental O2 >10 litres per minute or mechanical ventilation on admission
  2. Pregnancy
  3. AST/ALT > 5 times the upper limit normal
  4. Baseline prolonged QT
  5. Child-Pugh Score B or greater
  6. ESRD(end-stage renal disease) requiring dialysis
  7. Known allergy to medication component,
  8. History of severe G6PD (glucose-6-phosphate dehydrogenase)
  9. Myasthenia gravis
  10. Porphyria
  11. Ongoing treatment for epilepsy
  12. Life expectancy < 6 months,
  13. Patient lacks capacity to provide consent and does not have a surrogate decision maker.
  14. Retinal Disease

Sites / Locations

  • Kootenai Health

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Hydroxychloroquine (HCQ)

Usual Care

Arm Description

Initial dose: HCQ 400mg x 2 (800mg) then 200mg by mouth, three times per day (600mg/24hr period) starting 8 hours after the initial dose for a total of 14 doses over 5 days Plus Usual Care (See below for full description)

The care of hospitalized patients with covid-19 is evolving with hospital guidelines arising across the U.S. with several commonalities. Patients receive clinical assessment, chest x-ray, covid-19 testing, basic labs (WBC, CMP), and additional labs based on protocol or clinical judgment (ABG, CRP, LDH), antibiotics for possible bacterial pneumonia, acetaminophen for fever, supplemental O2, and consideration for mechanical ventilation. Early intubation over escalating noninvasive support. Low tidal volume ventilation and prone positioning are lung protective strategies used in critically ill covid-19 patients that are based on management of acute respiratory distress syndrome generally. Conservative fluid replacement is used to avoid worsening oxygenation.

Outcomes

Primary Outcome Measures

Change from Baseline Oxygenation on Day 1 to Day 5
paO2
Change from Baseline Oxygenation at Day 5
FIO2

Secondary Outcome Measures

Intensive Care length of stay
Length in hours
Required Mechanical Ventilation
Length in hours
Required Oxygen supplementation
Length in hours
Hospitalization length of Stay
Length in hours
Mortality
Date of Death
Cardiac Arrhythmia - Polymorphic Ventricular Tachycardia
Cardiologist Diagnostic Documentation
Cardiac Arrhythmia - Ventricular Tachycardia
Cardiologist Diagnostic Documentation
Cardiac Arrhythmia - Lengthening QTc
Cardiologist Diagnostic Documentation

Full Information

First Posted
April 14, 2020
Last Updated
February 4, 2021
Sponsor
Kootenai Health
Collaborators
Washington State University
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1. Study Identification

Unique Protocol Identification Number
NCT04382625
Brief Title
Hydroxychloroquine in SARS-CoV-2 (COVID-19) Pneumonia Trial
Official Title
Hydroxychloroquine in SARS-CoV-2 (COVID-19) Pneumonia Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2020
Overall Recruitment Status
Withdrawn
Why Stopped
Secondary to other study results, suspended for a scientific review
Study Start Date
October 2020 (Anticipated)
Primary Completion Date
January 1, 2022 (Anticipated)
Study Completion Date
June 1, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Kootenai Health
Collaborators
Washington State University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Novel coronavirus SARS(Severe Acute Respiratory Syndrome)-CoV-2 was first identified during the outbreak in Wuhan, China in December 2019 with the now resulting pandemic. Aggressive supportive care is the mainstay of treatment currently and rescue with lung protective mechanical ventilation is essential for survival in patients with severe acute respiratory distress syndrome. Despite supportive care, mortality is significant in hospitalized patients in the U.S., especially among patients > 65 years of age. Pharmacologic treatments to decrease disease severity are urgently needed. Hydroxychloroquine is currently widely used for treatment of autoimmune disease including systemic lupus erythematosus and rheumatoid arthritis, and it has been used to prevent and treat malaria. In vitro and in vivo antiviral activity towards SARS-CoV-2 has been reported. Since hydroxychloroquine has been used for decades its properties as a drug are well known. The investigators propose a pragmatic trial of hydroxychloroquine in moderately ill hospitalized adults with SARS-CoV-2 pneumonia with the hypothesis that hydroxychloroquine reduces severity of acute lung injury caused by SARS-CoV-2 infection.
Detailed Description
Novel coronavirus SARS-CoV-2 was first identified during the outbreak in Wuhan, China in December 2019 with the now resulting pandemic. Aggressive supportive care is the mainstay of treatment currently and rescue with lung protective mechanical ventilation is essential for survival in patients with severe acute respiratory distress syndrome. Despite supportive care, mortality is significant in hospitalized patients in the U.S., especially among patients > 65 years of age. Pharmacologic treatments to decrease disease severity are urgently needed. Candidate treatments with antiviral activity and/or immune-modulating effects include hydroxychloroquine (HCQ), lopinavir/ritonavir, remdesivir, and tocilizumab among others. There is limited high quality clinical data prompting a dilemma of how to use and review potential treatments and ensure patient safety now as the pandemic begins to peak. There are also significant limitations in drug supplies at many institutions. Hydroxychloroquine is currently widely used for treatment of autoimmune disease including systemic lupus erythematosus and rheumatoid arthritis, and it has been used to prevent and treat malaria. In vitro and in vivo antiviral activity towards SARS-CoV-2 has been reported. Since hydroxychloroquine has been used for decades its properties as a drug are well known. Pertinent adverse events to monitor in a hospitalized patient include QTc (corrected QT interval) prolongation, elevation of liver enzymes/acute liver injury, and hypokalemia. Acute lung injury and progressive respiratory failure is the major cause of mortality in SARS-CoV-2 infection. In acute lung injury and respiratory distress syndrome, the severity of hypoxia is categorized by the Pao2/FIO2 (fraction of inspired oxygen) ration as mild (200 mm Hg<Pao2/Fio2≤300 mm Hg), moderate (100 mm Hg<Pao2/Fio2≤200 mm Hg), and severe (Pao2/Fio2 ≤100 mm Hg). A persistently low Pao2/Fio2 ratio is associated with worse outcomes and may be a marker of failure to respond to conventional therapy. PaO2/FIO2 is a clinically useful measure in patients regardless of if they are receiving noninvasive supplemental O2 or mechanical ventilation, and low ratios are associated with duration of ICU stay and hospital mortality. The care of hospitalized patients with covid-19 is evolving with hospital guidelines arising across the U.S. with several commonalities. Patients receive clinical assessment, chest x-ray, covid-19 testing, basic labs (WBC, CMP), and additional labs based on protocol or clinical judgment (ABG, CRP-C reactive protein, LDH), antibiotics for possible bacterial pneumonia, acetaminophen for fever, supplemental O2, close monitoring for worsening respiratory status and consideration for mechanical ventilation. Since covid-19 is a novel illness, there is no proven clinically efficacious drug treatment. Candidate drugs are being used, some in the context of trials and others by physician discretion. Early intubation over escalating noninvasive support (ie. High flow nasal canula and bipap) has been adopted due to the frequency of rapidly worsening oxygenation, hemodynamic instability, and to protect staff from virus aerosolization. Low tidal volume ventilation and prone positioning are lung protective strategies used in critically ill covid-19 patients that are based on management of acute respiratory distress syndrome generally. Arrhythmias, cardiomyopathy, and shock are serious complications from covid-19 that warrant avoidance of acidosis, electrolyte monitoring and replacement, and pressor support. Conservative fluid replacement is used to avoid worsening oxygenation. In sum, multiple factors including timeliness and quality of care likely affect patient outcomes. Hospitalists and pulmonary critical care physicians direct the care of covid-19 patients with support from specialists as needed including infectious disease, cardiology, and nephrology. Pragmatic trials focus on studying the real-world effect of an intervention, such as a medication, in the context of other care a patient is likely to receive. The intervention is delivered by staff normally taking care of the patient with monitoring that is routinely available. Advantages can include generalizability, increased physician participation due to less burdensome study protocols, and feasibility. Disadvantages include allowance of unblinded design, bias from physicians and patients about the intervention, and more heterogeneity in treatment than in a mechanistic protocolized trial. Efforts to minimize bias include selecting objective outcomes (e.g. PaO2/FIO2 rather than cough or dyspnea).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
SARS-CoV-2 Pneumonia, COVID-19
Keywords
SARS-CoV-2, Pneumonia, Hydroxychloroquine, COVID-19

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Single-center pragmatic randomized open-label trial of hydroxychloroquine + usual care in hospitalized adults with confirmed SARS-CoV-2 infection and acute hypoxia compared to usual care.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Hydroxychloroquine (HCQ)
Arm Type
Experimental
Arm Description
Initial dose: HCQ 400mg x 2 (800mg) then 200mg by mouth, three times per day (600mg/24hr period) starting 8 hours after the initial dose for a total of 14 doses over 5 days Plus Usual Care (See below for full description)
Arm Title
Usual Care
Arm Type
No Intervention
Arm Description
The care of hospitalized patients with covid-19 is evolving with hospital guidelines arising across the U.S. with several commonalities. Patients receive clinical assessment, chest x-ray, covid-19 testing, basic labs (WBC, CMP), and additional labs based on protocol or clinical judgment (ABG, CRP, LDH), antibiotics for possible bacterial pneumonia, acetaminophen for fever, supplemental O2, and consideration for mechanical ventilation. Early intubation over escalating noninvasive support. Low tidal volume ventilation and prone positioning are lung protective strategies used in critically ill covid-19 patients that are based on management of acute respiratory distress syndrome generally. Conservative fluid replacement is used to avoid worsening oxygenation.
Intervention Type
Drug
Intervention Name(s)
Hydroxychloroquine
Other Intervention Name(s)
Plaquenil
Intervention Description
Hydroxychloroquine is currently widely used for treatment of autoimmune disease including systemic lupus erythematosus and rheumatoid arthritis, and it has been used to prevent and treat malaria.
Primary Outcome Measure Information:
Title
Change from Baseline Oxygenation on Day 1 to Day 5
Description
paO2
Time Frame
Day 1 of treatment to day 5 of treatment
Title
Change from Baseline Oxygenation at Day 5
Description
FIO2
Time Frame
Day 1 of treatment to day 5 of treatment
Secondary Outcome Measure Information:
Title
Intensive Care length of stay
Description
Length in hours
Time Frame
Day 0 to Day 28
Title
Required Mechanical Ventilation
Description
Length in hours
Time Frame
Day 0 to Day 28
Title
Required Oxygen supplementation
Description
Length in hours
Time Frame
Day 0 to Day 28
Title
Hospitalization length of Stay
Description
Length in hours
Time Frame
Day 0 to Day 28
Title
Mortality
Description
Date of Death
Time Frame
Day 0 to Day 28
Title
Cardiac Arrhythmia - Polymorphic Ventricular Tachycardia
Description
Cardiologist Diagnostic Documentation
Time Frame
Day 0 to Day 28
Title
Cardiac Arrhythmia - Ventricular Tachycardia
Description
Cardiologist Diagnostic Documentation
Time Frame
Day 0 to Day 28
Title
Cardiac Arrhythmia - Lengthening QTc
Description
Cardiologist Diagnostic Documentation
Time Frame
Day 0 to Day 28

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age > 18 years of age SARS-CoV-2 positive per FDA approved RT-PCR (reverse transcription-polymerase chain reaction) Acute hypoxia (O2 sat < 90 % or paO2 < 60 on room air), or above baseline chronic O2 requirement Inpatient admission Exclusion Criteria: Requires supplemental O2 >10 litres per minute or mechanical ventilation on admission Pregnancy AST/ALT > 5 times the upper limit normal Baseline prolonged QT Child-Pugh Score B or greater ESRD(end-stage renal disease) requiring dialysis Known allergy to medication component, History of severe G6PD (glucose-6-phosphate dehydrogenase) Myasthenia gravis Porphyria Ongoing treatment for epilepsy Life expectancy < 6 months, Patient lacks capacity to provide consent and does not have a surrogate decision maker. Retinal Disease
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sean Cook, D.O.
Organizational Affiliation
Kootenai Health
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jeanette Berg, MD, PhD
Organizational Affiliation
Kootenai Health
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Sterling McPherson, PhD
Organizational Affiliation
Washington State University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
John Roll, PhD
Organizational Affiliation
Washington State University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kootenai Health
City
Coeur d'Alene
State/Province
Idaho
ZIP/Postal Code
83814
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Hydroxychloroquine in SARS-CoV-2 (COVID-19) Pneumonia Trial

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