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Clinical Trials/NCT04570462
NCT04570462
Withdrawn
Not Applicable

Application of Mild Hypothermia for COVID-19 Acute Respiratory Distress

Northwell Health1 site in 1 countryMay 18, 2020
ConditionsCOVID19 ARDS

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
COVID19 ARDS
Sponsor
Northwell Health
Locations
1
Primary Endpoint
Changes in metabolic requirement during and after hypothermia
Status
Withdrawn
Last Updated
4 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
May 18, 2020
End Date
December 31, 2020
Last Updated
4 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Pey-Jen Yu, MD

Director, Clinical Research Programs, Department of Cardiovascular and Thoracic Surgery, North Shore University Hospital, Northwell Health

Northwell Health

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

Outcomes

Primary Outcomes

Changes in metabolic requirement during and after hypothermia

Time Frame: Every 12 hours through study completion an average of 4 days

indirect calorimeter measurements (Kcal/day)

Secondary Outcomes

  • Changes in oxygen requirements and levels during and after hypothermia(Every 12 hours through study completion, an average of 4 days)
  • length of intubation(through study completion, an average of 4 days)
  • Changes in carbon dioxide levels during and after hypothermia(Every 12 hours through study completion an average of 4 days)
  • does application of hypothermia reduce pro inflammatory response(through study completion an average of 4 days)

Study Sites (1)

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