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Hyperbaric Oxygen as an Adjuvant Treatment for Patients With Covid-19 Severe Hypoxemia

Primary Purpose

Covid19

Status
Terminated
Phase
Phase 2
Locations
Argentina
Study Type
Interventional
Intervention
Hyperbaric Oxygen
Sponsored by
Asociación Argentina de Medicina Hiperbárica e Investigación
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Covid19 focused on measuring Hyperbaric Oxygen, Covid-19, Hypoxemia, Sars-CoV2, Hyperbaric Chamber

Eligibility Criteria

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

Inclusion Criteria:

  • 18 years, all sexes.
  • No previous hospitalizations in the last 6 months.
  • Positive diagnostic test for COVID-19 according to the guidelines of the Argetine Ministry of Health at the time of enrollment.
  • Patient in Intensive Care Unit with oxygen need: Need for continuous supply of oxygen to maintain saturation by oximetry pulse (SpO2) greater than or equal to 93% or arterial gas with PaO2 value greater than 60 mmHg

Exclusion Criteria:

  • 18 years of age.
  • Person unable to give consent.
  • Person who refuses to participate.
  • Pregnancy and lactation
  • Participating in other study
  • Requirement for mechanical ventilation.
  • Inability to maintain prolonged sitting position (at least 2 hours)
  • Subject with contraindications to HBOT (pulmonary shock, bullae, emphysema or untreated pneumothorax, severe seizures, uncontrolled hypertension, chronic obstructive disease of grade III or IV).

Sites / Locations

  • Hospital Central de San Isidro Dr. Angel Melchor Posse
  • Hospital de Infecciosas F. J. Muñiz
  • Hospital General de Agudos D.F Santojanni

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Experimental HBOT

Standard care

Arm Description

Treatment (device). Patients will receive 90 minutes of hyperbaric oxygen at 1,45 ATA in a Revitalair430 hyperbaric chamber, and then they will continue with standard care and normobaric oxygen.

Outcomes

Primary Outcome Measures

Time to normalize the oxygen requirement (oxygen dependence)
Time to normalize the oxygen requirement: Allowing a pulse oximetry value in ambient air greater than or equal 93% and/or arterial blood gas with PaO2 value greater than 60 mmHg in ambient air.

Secondary Outcome Measures

Need for Invasive Mechanical Ventilation (IMV) and / or Respiratory Distress Syndrome Acute (ARDS)
Number of patients who required IMV after being enrolled
Development of Acute Respiratory Distress Syndrome (ARDS)
Number of patients who required IMV and / or had a diagnosis of ARDS after being enrolled.
30-day mortality
Number of patients who died in that period since enrollment
Hypotension with vasopressor requirement
Number of patients with hypotension who were administered vasopressors in this period
Mortality
Number of patients who died in that period since enrollment.

Full Information

First Posted
July 16, 2020
Last Updated
January 13, 2021
Sponsor
Asociación Argentina de Medicina Hiperbárica e Investigación
Collaborators
Hospital de Infecciosas Francisco Javier Muniz, Hospital General de Agudos D. F. Santojanni, Hospital Central de San Isidro Dr. Melchor Angel Posse
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1. Study Identification

Unique Protocol Identification Number
NCT04477954
Brief Title
Hyperbaric Oxygen as an Adjuvant Treatment for Patients With Covid-19 Severe Hypoxemia
Official Title
Hyperbaric Oxygen as an Adjuvant Treatment for Patients With Covid-19 Severe Hypoxemia
Study Type
Interventional

2. Study Status

Record Verification Date
January 2021
Overall Recruitment Status
Terminated
Why Stopped
Investigators and Ethic Committee endorsed early suspension of the protocol because of superiority and safety. For the interim analysys, the statistical methodology presented by Pocock was followed.
Study Start Date
July 6, 2020 (Actual)
Primary Completion Date
November 6, 2020 (Actual)
Study Completion Date
December 30, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Asociación Argentina de Medicina Hiperbárica e Investigación
Collaborators
Hospital de Infecciosas Francisco Javier Muniz, Hospital General de Agudos D. F. Santojanni, Hospital Central de San Isidro Dr. Melchor Angel Posse

4. Oversight

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

5. Study Description

Brief Summary
The severity of COVID-19 is related to the level of hypoxemia, respiratory failure, how long it lasts and how refractory it is at increasing concentrations of inspired oxygen. The inability to perform hematosis due to edema that occurs from acute inflammation could be attenuated by the administration of hyperbaric oxygen (HBO). Recently, it has been reported benefits in this matter in patients with SARS-CoV-2 hypoxemic pneumonia in China; where the administration of repeated HBO sessions decreased the need for mechanical ventilation (MV) in patients admitted to the Intensive Care Unit due to COVID-19. Hyperbaric oxygen is capable of increasing drastically the amount of dissolved oxygen in the blood and maintain an adequate supply oxygen to the tissues. In addition to this, it can influence immune processes, both humoral and cellular, allowing to reduce the intensity of the response inflammatory and stimulate antioxidant defenses. HBO is considered safe and it has very few adverse events, it is a procedure approved by our authorities regulatory for several years. In the current context of the pandemic by COVID-19 and worldwide reports of mortality associated with severe cases of respiratory failure, it is essential to propose therapeutical strategies to limit or decrease respiratory compromise of severe stages by COVID-19. That is why, it is proposed to carry out this research to assess whether HBO treatment can improve the evolution of patients with COVID-19 severe hypoxemia.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Covid19
Keywords
Hyperbaric Oxygen, Covid-19, Hypoxemia, Sars-CoV2, Hyperbaric Chamber

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Model Description
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Experimental HBOT
Arm Type
Experimental
Arm Description
Treatment (device). Patients will receive 90 minutes of hyperbaric oxygen at 1,45 ATA in a Revitalair430 hyperbaric chamber, and then they will continue with standard care and normobaric oxygen.
Arm Title
Standard care
Arm Type
No Intervention
Intervention Type
Combination Product
Intervention Name(s)
Hyperbaric Oxygen
Other Intervention Name(s)
HBOT
Intervention Description
Hyperbaric oxygen therapy (HBOT): inhalation of pressurized oxygen through a hyperbaric chamber (Revitalair430)
Primary Outcome Measure Information:
Title
Time to normalize the oxygen requirement (oxygen dependence)
Description
Time to normalize the oxygen requirement: Allowing a pulse oximetry value in ambient air greater than or equal 93% and/or arterial blood gas with PaO2 value greater than 60 mmHg in ambient air.
Time Frame
15-30 days.
Secondary Outcome Measure Information:
Title
Need for Invasive Mechanical Ventilation (IMV) and / or Respiratory Distress Syndrome Acute (ARDS)
Description
Number of patients who required IMV after being enrolled
Time Frame
30 days
Title
Development of Acute Respiratory Distress Syndrome (ARDS)
Description
Number of patients who required IMV and / or had a diagnosis of ARDS after being enrolled.
Time Frame
30 days
Title
30-day mortality
Description
Number of patients who died in that period since enrollment
Time Frame
30 days
Title
Hypotension with vasopressor requirement
Description
Number of patients with hypotension who were administered vasopressors in this period
Time Frame
30 days
Title
Mortality
Description
Number of patients who died in that period since enrollment.
Time Frame
45 days / 60 days / 90 days and 180 days
Other Pre-specified Outcome Measures:
Title
Adverse events
Description
Number of adverse events reported related to the device (Revitalair 430 hyperbaric chamber): otalgias, ear obstruction, barotrauma, significant and constant changes in blood pressure, heart rate and others
Time Frame
4 hours finished session

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 18 years, all sexes. No previous hospitalizations in the last 6 months. Positive diagnostic test for COVID-19 according to the guidelines of the Argetine Ministry of Health at the time of enrollment. Patient in Intensive Care Unit with oxygen need: Need for continuous supply of oxygen to maintain saturation by oximetry pulse (SpO2) greater than or equal to 93% or arterial gas with PaO2 value greater than 60 mmHg Exclusion Criteria: 18 years of age. Person unable to give consent. Person who refuses to participate. Pregnancy and lactation Participating in other study Requirement for mechanical ventilation. Inability to maintain prolonged sitting position (at least 2 hours) Subject with contraindications to HBOT (pulmonary shock, bullae, emphysema or untreated pneumothorax, severe seizures, uncontrolled hypertension, chronic obstructive disease of grade III or IV).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mariana Cannellotto, MD
Organizational Affiliation
Asociación Argentina de Medicina Hiperbárica e Investigación
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Mariano Duarte, PhD
Organizational Affiliation
Asociación Argentina de Medicina Hiperbárica e Investigación
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Liliana Jorda-Vargas
Organizational Affiliation
Asociación Argentina de Medicina Hiperbárica e Investigación
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Fabrizio Verdini, MD
Organizational Affiliation
Asociación Argentina de Medicina Hiperbárica e Investigación
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Central de San Isidro Dr. Angel Melchor Posse
City
San Isidro
State/Province
Buenos Aires
ZIP/Postal Code
1641
Country
Argentina
Facility Name
Hospital de Infecciosas F. J. Muñiz
City
Ciudad Autonoma de Buenos AIres
State/Province
Caba
ZIP/Postal Code
1282
Country
Argentina
Facility Name
Hospital General de Agudos D.F Santojanni
City
Ciudad Autonoma de Buenos AIres
State/Province
Caba
ZIP/Postal Code
1408
Country
Argentina

12. IPD Sharing Statement

Plan to Share IPD
No

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Hyperbaric Oxygen as an Adjuvant Treatment for Patients With Covid-19 Severe Hypoxemia

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