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Hyperbaric Versus Normobaric Oxygen Therapy for COVID-19 Patients

Primary Purpose

Covid19

Status
Unknown status
Phase
Phase 2
Locations
Canada
Study Type
Interventional
Intervention
Oxygen
Sponsored by
Ottawa Hospital Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Covid19 focused on measuring Hyperbaric oxygen therapy

Eligibility Criteria

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

Inclusion Criteria:

  • Male or non-pregnant female patients
  • Age ≥18 years
  • Confirmed COVID-19 positive by RT-PCR or another validated method
  • Diagnosed with pneumonia requiring 21%<FIO2≤100% to maintain saturation by pulse oximetry (SpO2) ≥90%
  • Able and willing to comply with study procedures and follow-up examinations contained within the written consent form

Exclusion Criteria:

  • Patient clinical status felt to be incompatible with HBOT, e.g. respiratory failure requiring mechanical ventilation
  • Pregnancy, determined by a serum or urine test
  • Hemodynamic instability requiring vasopressors
  • Inability to maintain a sitting position during treatment
  • Inability to effectively understand and communicate with the hyperbaric operator, or to give consent
  • Inability to spontaneously equalize ears and refusal of myringotomies
  • Contraindications to HBOT (e.g. pneumothorax)

Sites / Locations

  • The Ottawa Hospital
  • Rouge Valley Hyperbaric Medical CentreRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

HBOT

Control

Arm Description

These patients will receive hyperbaric oxygen therapy (HBOT) in addition to usual treatment for COVID-19. HBOT sessions will be 75 minutes in length at a pressure of 2.0 ATA.

These patients will receive usual treatment for COVID-19, including oxygenation at normal atmospheric pressure (normobaric oxygenation).

Outcomes

Primary Outcome Measures

7-level COVID Ordinal Outcome Scale
7-level scale based on patient's current status and need for oxygenation, also ability to resume normal activities (at higher levels). Range is 1-7. Higher number indicates better clinical outcome.

Secondary Outcome Measures

Length of hospital stay
Measured in days
Days with oxygen supplementation
Number of days with oxygen supplementation
Daily oxygen flow values required to obtain saturation values ≥90%,
Measured in L/min
ICU admission
Yes/No
ICU length of stay
Measured in days, if applicable
Days on invasive mechanical ventilation or high flow oxygenation
Number of days on ventilator
Major arterial and venous thrombotic events
e.g. stroke, pulmonary embolism, deep vein thrombosis
Sleep quality
Sleep Quality Scale, measured from 0 to 10. Higher number indicates worse sleep quality: 0 = "best possible sleep", 10 = "worst possible sleep". Capelleri et. al; Health and Quality of Life Outcomes 2009: 7:54
Fatigue
Single-Item Fatigue Report Mark, measured from 1 to 10. Higher number indicates worse fatigue: 1 = "not at all", 10 = "extremely". van Hooff et al; J Occup Health 2007; 49:224-234.
7-level COVID Ordinal Outcome Scale
Same scale as the primary outcome; different timing as a secondary outcome. Range is 1-7. Higher number indicates better clinical outcome.
Mortality
Number of deaths
Incidence of any adverse events related to HBOT
Number of adverse events

Full Information

First Posted
July 31, 2020
Last Updated
October 29, 2021
Sponsor
Ottawa Hospital Research Institute
Collaborators
Climate Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT04500626
Brief Title
Hyperbaric Versus Normobaric Oxygen Therapy for COVID-19 Patients
Official Title
Multicentre Randomized Controlled Trial of Hyperbaric Versus Normobaric Oxygen Therapy for COVID-19 Patients
Study Type
Interventional

2. Study Status

Record Verification Date
October 2021
Overall Recruitment Status
Unknown status
Study Start Date
April 15, 2021 (Actual)
Primary Completion Date
August 2022 (Anticipated)
Study Completion Date
August 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Ottawa Hospital Research Institute
Collaborators
Climate Foundation

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
At least 1 in 6 COVID-19 patients admitted to hospital to receive extra oxygen will die of complications. In patients with COVID-19, invasive treatment such as mechanical ventilation (e.g. breathing with a machine) is associated with a 50% increased risk of death. Invasive treatments use a lot of healthcare resources in intensive care units and may lead to further deaths if patients do not have access to care. The investigators aim to improve outcomes for COVID-19 patients by implementing hyperbaric oxygen therapy (HBOT). HBOT allows patients to breathe 100% oxygen in a special chamber at a pressure higher than sea level. It is approved by Health Canada for 14 conditions. HBOT is safe when administered by experienced teams. There are two main causes of death in severe COVID-19 respiratory infections: (i) a decreased diffusion of oxygen from the lungs to the blood and (ii) an increased inflammatory response (also called a "cytokine storm"). HBOT leads to increased oxygen level in blood, has strong anti-inflammatory effects, and may destroy the virus responsible for COVID-19 disease. The initial experience with HBOT and COVID-19 from China, France and the United States is promising in that it prevents further worsening of the condition and need for intensive care. The investigators propose to test the effectiveness of HBOT for COVID-19 patients who are admitted to hospital to receive extra oxygen. Using the most rigorous and innovative research methods, this Canadian-led international study will operate at 5 centers across 3 countries (Canada: Ottawa, Toronto, Edmonton; Switzerland: Geneva; UK: Rugby/London). The investigators anticipate that when treated by HBOT, COVID-19 patients needing extra oxygen to breathe will see significant health improvements as well as a decrease in complications, inflammation in the blood, need for invasive care, death, and cost of care.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Covid19
Keywords
Hyperbaric oxygen therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
234 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
HBOT
Arm Type
Experimental
Arm Description
These patients will receive hyperbaric oxygen therapy (HBOT) in addition to usual treatment for COVID-19. HBOT sessions will be 75 minutes in length at a pressure of 2.0 ATA.
Arm Title
Control
Arm Type
No Intervention
Arm Description
These patients will receive usual treatment for COVID-19, including oxygenation at normal atmospheric pressure (normobaric oxygenation).
Intervention Type
Drug
Intervention Name(s)
Oxygen
Intervention Description
Hyperbaric oxygen therapy delivered in a monoplace or multi-place chamber. Supervised by a hyperbaric oxygen therapy physician and a chamber operator.
Primary Outcome Measure Information:
Title
7-level COVID Ordinal Outcome Scale
Description
7-level scale based on patient's current status and need for oxygenation, also ability to resume normal activities (at higher levels). Range is 1-7. Higher number indicates better clinical outcome.
Time Frame
Measured on Day 7
Secondary Outcome Measure Information:
Title
Length of hospital stay
Description
Measured in days
Time Frame
Duration of study (to Day 28)
Title
Days with oxygen supplementation
Description
Number of days with oxygen supplementation
Time Frame
Duration of study (to Day 28)
Title
Daily oxygen flow values required to obtain saturation values ≥90%,
Description
Measured in L/min
Time Frame
Duration of study (to Day 28)
Title
ICU admission
Description
Yes/No
Time Frame
Duration of study (to Day 28)
Title
ICU length of stay
Description
Measured in days, if applicable
Time Frame
Duration of study (to Day 28)
Title
Days on invasive mechanical ventilation or high flow oxygenation
Description
Number of days on ventilator
Time Frame
Duration of study (to Day 28)
Title
Major arterial and venous thrombotic events
Description
e.g. stroke, pulmonary embolism, deep vein thrombosis
Time Frame
Duration of study (to Day 28)
Title
Sleep quality
Description
Sleep Quality Scale, measured from 0 to 10. Higher number indicates worse sleep quality: 0 = "best possible sleep", 10 = "worst possible sleep". Capelleri et. al; Health and Quality of Life Outcomes 2009: 7:54
Time Frame
Duration of study (to Day 28)
Title
Fatigue
Description
Single-Item Fatigue Report Mark, measured from 1 to 10. Higher number indicates worse fatigue: 1 = "not at all", 10 = "extremely". van Hooff et al; J Occup Health 2007; 49:224-234.
Time Frame
Duration of study (to Day 28)
Title
7-level COVID Ordinal Outcome Scale
Description
Same scale as the primary outcome; different timing as a secondary outcome. Range is 1-7. Higher number indicates better clinical outcome.
Time Frame
Measured on Day 28
Title
Mortality
Description
Number of deaths
Time Frame
Duration of study (to Day 28)
Title
Incidence of any adverse events related to HBOT
Description
Number of adverse events
Time Frame
Duration of study (to Day 28)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male or non-pregnant female patients Age ≥18 years Confirmed COVID-19 positive by RT-PCR or another validated method Diagnosed with pneumonia requiring 21%<FIO2≤100% to maintain saturation by pulse oximetry (SpO2) ≥90% Able and willing to comply with study procedures and follow-up examinations contained within the written consent form Exclusion Criteria: Patient clinical status felt to be incompatible with HBOT, e.g. respiratory failure requiring mechanical ventilation Pregnancy, determined by a serum or urine test Hemodynamic instability requiring vasopressors Inability to maintain a sitting position during treatment Inability to effectively understand and communicate with the hyperbaric operator, or to give consent Inability to spontaneously equalize ears and refusal of myringotomies Contraindications to HBOT (e.g. pneumothorax)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sylvain Boet, MD, PhD
Phone
613-737-8899
Ext
78187
Email
sboet@toh.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Joseph Burns, MSc
Phone
613-798-5555
Ext
14775
Email
josburns@ohri.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sylvain Boet, MD, PhD
Organizational Affiliation
The Ottawa Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Ottawa Hospital
City
Ottawa
State/Province
Ontario
ZIP/Postal Code
K1Y4E9
Country
Canada
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sylvain Boet, MD, PhD
Phone
6137985555
Ext
78187
Email
sboet@toh.on.ca
First Name & Middle Initial & Last Name & Degree
Joseph Burns, MSc
Phone
613-798-5555
Ext
14775
Email
josburns@ohri.ca
Facility Name
Rouge Valley Hyperbaric Medical Centre
City
Scarborough
State/Province
Ontario
ZIP/Postal Code
M1E 5E9
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rita Katznelson, MD
Email
rita.katznelson@uhn.ca
First Name & Middle Initial & Last Name & Degree
Research Coordinator
Email
research@centenarypainclinic.ca
First Name & Middle Initial & Last Name & Degree
Rita Katznelson, MD

12. IPD Sharing Statement

Plan to Share IPD
No
Links:
URL
https://www.medrxiv.org/content/10.1101/2020.07.15.20154609v1
Description
Preprint of study protocol (brief version for publication)

Learn more about this trial

Hyperbaric Versus Normobaric Oxygen Therapy for COVID-19 Patients

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