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Mild Hypothermia for COVID-19 ARDS

Primary Purpose

COVID19 ARDS

Status
Withdrawn
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Hypothermia Via Cooling Machine- Arctic Sun 5000
Sponsored by
Northwell Health
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for COVID19 ARDS

Eligibility Criteria

18 Years - 100 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Provision of signed and dated informed consent form from Legally Authorized Representative.
  2. Stated willingness to comply with all study procedures and availability for the duration of the study
  3. Male or female, aged 18 years or above
  4. COVID positive
  5. On mechanical ventilation with either: refractory respiratory acidosis (ph ≤ 7.20), hypercarbia (pCO2 ≥ 55 mmHg), refractory hypoxia (pO2/FIO2 <150), or plateau pressures >30

Exclusion Criteria:

  1. Bleeding (active bleeding, platelets less than 50,000)
  2. Uncontrolled cardiac arrhythmia
  3. History of cryoglobulinemia, major trauma, pregnancy
  4. Active non-COVID-19 infection that is not controlled with antibiotic or antifungal regimen

Sites / Locations

  • North Shore University Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Experimental Arm- Induction of Mild Hypothermia Protocol

Arm Description

Determination of metabolic rate by the metabolic cart (noninvasive connection of the device to the ventilator for 20 minutes). Initiate hypothermia (established Northwell hypothermia status post cardiac arrest protocol) using the Arctic Sun. The Arctic Sun 5000® is set to a temperature of 34.5 C to lower the body temperature.

Outcomes

Primary Outcome Measures

Changes in metabolic requirement during and after hypothermia
indirect calorimeter measurements (Kcal/day)

Secondary Outcome Measures

Changes in oxygen requirements and levels during and after hypothermia
ABG, PaO2 (mmHg)
length of intubation
number of hours intubated
Changes in carbon dioxide levels during and after hypothermia
measured by ABG, PaCO2 mmHg
does application of hypothermia reduce pro inflammatory response
ESR (mm/hr)
does application of hypothermia reduce pro inflammatory response
Ferritin (ng/ml)
does application of hypothermia reduce pro inflammatory response
D Dimer (ng/ml)

Full Information

First Posted
July 21, 2020
Last Updated
June 25, 2021
Sponsor
Northwell Health
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1. Study Identification

Unique Protocol Identification Number
NCT04570462
Brief Title
Mild Hypothermia for COVID-19 ARDS
Official Title
Application of Mild Hypothermia for COVID-19 Acute Respiratory Distress
Study Type
Interventional

2. Study Status

Record Verification Date
September 2020
Overall Recruitment Status
Withdrawn
Why Stopped
The study was opened at the close of the peak of COVID. At our institution, there are significantly less COVID patients admitted who qualify for the study
Study Start Date
May 18, 2020 (Actual)
Primary Completion Date
December 31, 2020 (Anticipated)
Study Completion Date
December 31, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Northwell Health

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
Some patients with COVID have abnormally high carbon dioxide and low oxygen levels despite being on the ventilator. The hypothesis of the study is that the application of mild hypothermia to patients with COVID will decrease their metabolic rate and improve their oxygenation and carbon dioxide levels.
Detailed Description
A significant contributor to the morbidity and mortality from COVID-19 is from the abnormal carbon dioxide and oxygen levels in COVID-19 patients. Metabolic studies done on COVID-19 patients have shown that these patients have abnormally high metabolic rates. High metabolic rates results in increased carbon dioxide production and increased oxygen usage, both of which can result in high carbon dioxide and low oxygen levels. As some patients with severe COVID-19 continue to have high carbon dioxide levels and/or low oxygen levels despite being on the ventilator, it is hypothesized that decreasing the metabolic rate in these COVID-19 patients will help their oxygen and carbon dioxide levels. Mild hypothermia is currently used in comatose survivors of cardiac arrest to improve mortality and neurological outcomes. Mild hypothermia is also an effective way to reduce metabolic demand. The aim is to apply mild hypothermia to COVID-19 patients to decrease metabolic rate in order to improve their oxygen and carbon dioxide levels. Although the application for mild hypothermia has been widely adopted in some patient populations, it has never been applied in COVID-19 patients. If we can develop a strategy to help improve the oxygen and carbon dioxide levels in COVID-19 patients, it may lead to improvements in their overall outcomes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
COVID19 ARDS

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Experimental Arm- Induction of Mild Hypothermia Protocol
Arm Type
Experimental
Arm Description
Determination of metabolic rate by the metabolic cart (noninvasive connection of the device to the ventilator for 20 minutes). Initiate hypothermia (established Northwell hypothermia status post cardiac arrest protocol) using the Arctic Sun. The Arctic Sun 5000® is set to a temperature of 34.5 C to lower the body temperature.
Intervention Type
Other
Intervention Name(s)
Hypothermia Via Cooling Machine- Arctic Sun 5000
Intervention Description
Initiate hypothermia using the Arctic Sun.The Arctic Sun 5000® is set to a temperature of 34.5 C to lower the body temperature. Duration of hypothermia will be 48 hours after which the subject will be rewarmed. Metabolic rate, or indirect Calorimetry, will be assessed at baseline, day 1 of hypothermia, day 2 of hypothermia before rewarming, and after full rewarming. CBC, basic metabolic profile, magnesium, phosphorus, coagulation profile, ABG, inflammatory markers would be drawn every 12 hours during hypothermia until subject has achieved full rewarming and once after full rewarming. The entire hypothermia procedure will last 48 hours. Acceptable rewarming range is a temperature of 36.5C to 37.5C. The subject body temperature rewarming is typically set over 6-8 hours. Therefore, the final 6-8 hours of the 48 hour time period is set to rewarm the subject.
Primary Outcome Measure Information:
Title
Changes in metabolic requirement during and after hypothermia
Description
indirect calorimeter measurements (Kcal/day)
Time Frame
Every 12 hours through study completion an average of 4 days
Secondary Outcome Measure Information:
Title
Changes in oxygen requirements and levels during and after hypothermia
Description
ABG, PaO2 (mmHg)
Time Frame
Every 12 hours through study completion, an average of 4 days
Title
length of intubation
Description
number of hours intubated
Time Frame
through study completion, an average of 4 days
Title
Changes in carbon dioxide levels during and after hypothermia
Description
measured by ABG, PaCO2 mmHg
Time Frame
Every 12 hours through study completion an average of 4 days
Title
does application of hypothermia reduce pro inflammatory response
Description
ESR (mm/hr)
Time Frame
through study completion an average of 4 days
Title
does application of hypothermia reduce pro inflammatory response
Description
Ferritin (ng/ml)
Time Frame
through study completion an average of 4 days
Title
does application of hypothermia reduce pro inflammatory response
Description
D Dimer (ng/ml)
Time Frame
through study completion an average of 4 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
100 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Provision of signed and dated informed consent form from Legally Authorized Representative. Stated willingness to comply with all study procedures and availability for the duration of the study Male or female, aged 18 years or above COVID positive On mechanical ventilation with either: refractory respiratory acidosis (ph ≤ 7.20), hypercarbia (pCO2 ≥ 55 mmHg), refractory hypoxia (pO2/FIO2 <150), or plateau pressures >30 Exclusion Criteria: Bleeding (active bleeding, platelets less than 50,000) Uncontrolled cardiac arrhythmia History of cryoglobulinemia, major trauma, pregnancy Active non-COVID-19 infection that is not controlled with antibiotic or antifungal regimen
Facility Information:
Facility Name
North Shore University Hospital
City
Manhasset
State/Province
New York
ZIP/Postal Code
11030
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Mild Hypothermia for COVID-19 ARDS

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