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Nitric Oxide Inhalation Therapy for COVID-19 Infections in the ED (NO COV-ED)

Primary Purpose

COVID19

Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Nitric Oxide Gas
Inhaled Supplemental Oxygen
Sponsored by
Massachusetts General Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for COVID19 focused on measuring inhaled nitric oxide, emergency department, emergency medicine, respiratory infection

Eligibility Criteria

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

Inclusion Criteria:

  • Age ≥ 18 years old
  • Presentation to the ED with respiratory symptoms likely caused by COVID-19
  • Patient displays at least one of the following

    1. respiratory rate ≥ 24
    2. new cough
    3. new atypical chest pain
    4. new dyspnea
    5. oxygen saturation < 97% at rest
    6. chest x-ray with new changes consistent with COVID-related airspace disease
  • Cleared for discharge home by attending physician
  • Obtained COVID testing (results not required at time of enrollment)
  • Onset of symptoms ≤12 days prior to ED visit

Exclusion Criteria:

  • Attending physician estimation (< 50% likelihood) of other more likely non-COVID etiology
  • Presence of tracheostomy
  • Requirement of oxygen therapy to maintain resting oxygen saturation of > 94%
  • Clinical contraindication to use of inhaled nitric oxide

Sites / Locations

  • Massachusetts General Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Treatment Group

Control Group

Arm Description

Inhaled nitric oxide

Inhaled supplemental oxygen

Outcomes

Primary Outcome Measures

Rates of return visits to the ED
Difference within treatment and control groups with COVID-related symptoms/disease in their likelihood to return to the ED with worsening symptoms

Secondary Outcome Measures

Inpatient hospitalizations required
Difference within treatment and control groups with COVID-related symptoms/disease in their likelihood to require hospitalization during their COVID-19 course
Rates of intubation
Difference within treatment and control groups with COVID-related symptoms/disease in their likelihood to require intubation during their COVID-19 course
Rates of mortality
Difference within treatment and control groups with COVID-related symptoms/disease in their likelihood to die of any cause within 28 days of their initial ED visit

Full Information

First Posted
April 5, 2020
Last Updated
December 15, 2021
Sponsor
Massachusetts General Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04338828
Brief Title
Nitric Oxide Inhalation Therapy for COVID-19 Infections in the ED
Acronym
NO COV-ED
Official Title
Nitric Oxide Inhalation Therapy for COVID-19 Infections in the Emergency Department
Study Type
Interventional

2. Study Status

Record Verification Date
December 2021
Overall Recruitment Status
Terminated
Why Stopped
Absence of patients meeting criteria following initial COVID surge. DMSB recommended analysis of results to date and early closure.
Study Start Date
April 18, 2020 (Actual)
Primary Completion Date
January 14, 2021 (Actual)
Study Completion Date
March 1, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Massachusetts General Hospital

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.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The spread of novel Coronavirus (2019-nCoV) related infection (COVID-19) has led to many patient presentations in the emergency department for respiratory complaints, with many of these patients requiring ICU admission and ventilatory support. While COVID-19 patients have an increased need for supportive care, there is currently no specific treatment directed against 2019-nCoV. Nitric oxide inhalation has been used as a pulmonary vasodilator and has been found to have antiviral activity against other coronavirus strains. The primary aim of this study is to determine whether inhaled NO improves short term respiratory status, prevents future hospitalization, and improves the clinical course in patients diagnosed with COVID-19 specifically in the emergency department.
Detailed Description
The spread of novel Coronavirus (2019-nCoV) related infection (COVID-19) has led to many patient presentations in the emergency department for respiratory complaints, with many of these patients requiring ICU admission and ventilatory support. While COVID-19 patients have an increased need for supportive care, there is currently no specific treatment directed against 2019-nCoV. Nitric oxide inhalation has been used as a pulmonary vasodilator and has been found to have antiviral activity against other coronavirus strains. Preliminary data support a microbicidal effect of high concentration inhaled NO. We hypothesize that high concentration inhaled NO can have a viricidal effect against SARS-Cov-2 and prevent the deterioration to a severe form of COVID-19 when administered at an early stage of the disease. Additional potential mechanisms why INO may be effective in this indication: 1)improves V/Q ratio, 2) reduces PVR and PAP, 3) Anti-thrombotic in lung. This would have potential benefit for the patients in terms of reducing the severity of the clinical course and time to recovery. An additional benefit could be for the society since a faster and a less severe clinical course could protect limited hospital resources (ED, floor, and ICU) from being overwhelmed. The primary aim is to prevent the deterioration of mild COVID-19 infection (defined by a RT-PCR positive for SARS-CoV-2 in a specimen from any site) with respiratory signs/ symptoms to a more severe form of the disease as defined by the patient needing to 1) return to the ED, 2) be admitting to the hospital, 3) be intubated, 4) and all cause 28 day mortality.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
COVID19
Keywords
inhaled nitric oxide, emergency department, emergency medicine, respiratory infection

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
47 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Treatment Group
Arm Type
Experimental
Arm Description
Inhaled nitric oxide
Arm Title
Control Group
Arm Type
Placebo Comparator
Arm Description
Inhaled supplemental oxygen
Intervention Type
Drug
Intervention Name(s)
Nitric Oxide Gas
Intervention Description
Inhaled NO administered at target inspired concentration 140 - 300 ppm for 20-30 minutes
Intervention Type
Other
Intervention Name(s)
Inhaled Supplemental Oxygen
Intervention Description
2 L/min oxygen therapy
Primary Outcome Measure Information:
Title
Rates of return visits to the ED
Description
Difference within treatment and control groups with COVID-related symptoms/disease in their likelihood to return to the ED with worsening symptoms
Time Frame
28 days
Secondary Outcome Measure Information:
Title
Inpatient hospitalizations required
Description
Difference within treatment and control groups with COVID-related symptoms/disease in their likelihood to require hospitalization during their COVID-19 course
Time Frame
28 days
Title
Rates of intubation
Description
Difference within treatment and control groups with COVID-related symptoms/disease in their likelihood to require intubation during their COVID-19 course
Time Frame
28 days
Title
Rates of mortality
Description
Difference within treatment and control groups with COVID-related symptoms/disease in their likelihood to die of any cause within 28 days of their initial ED visit
Time Frame
28 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥ 18 years old Presentation to the ED with respiratory symptoms likely caused by COVID-19 Patient displays at least one of the following respiratory rate ≥ 24 new cough new atypical chest pain new dyspnea oxygen saturation < 97% at rest chest x-ray with new changes consistent with COVID-related airspace disease Cleared for discharge home by attending physician Obtained COVID testing (results not required at time of enrollment) Onset of symptoms ≤12 days prior to ED visit Exclusion Criteria: Attending physician estimation (< 50% likelihood) of other more likely non-COVID etiology Presence of tracheostomy Requirement of oxygen therapy to maintain resting oxygen saturation of > 94% Clinical contraindication to use of inhaled nitric oxide
Facility Information:
Facility Name
Massachusetts General Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02114
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Nitric Oxide Inhalation Therapy for COVID-19 Infections in the ED

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