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Helmet CPAP Versus HFNC in COVID-19

Helmet CPAP Versus HFNC in COVID-19

Recruiting
18 years and older
All
Phase N/A

Overview

We aim to investigate whether the use of Continuous Positive Airway Pressure using a Helmet device (Helmet CPAP) will increase the number of days alive and free of ventilator within 28 days compared to the use of a High Flow Nasal Cannula (HFNC) in patients admitted to Helsingborg Hospital, Sweden, suffering from COVID-19 and an acute hypoxic respiratory failure.

Description

A detailed description can be found in the study protocol which is pending submission for peer-review.

Eligibility

Inclusion Criteria (all of the following):

  1. Age 18 years
  2. Sars-Cov-2 found in the upper or lower respiratory tract by PCR during the current disease episode
  3. Peripheral oxygen saturation (SpO2) < 92 % despite conventional low-flow oxygen therapy of at least 6 L /min for at least 15 min
  4. A decision to initiate HFNC or Helmet CPAP by the attending ward physician
  5. The patient has given written informed consent to participate.

Exclusion Criteria (any of the following):

  1. Need for direct admission to the intensive care unit for mechanical ventilation
  2. Unconsciousness or drowsiness
  3. Pneumothorax
  4. Carbon dioxide pressure (pCO2) > 6 kPa in venous blood gas (VBG)
  5. Underlying chronic obstructive pulmonary disease stage III-IV
  6. A decision not to participate
  7. Inability to comprehend the study content and give informed consent

Study details
    COVID
    Acute Hypoxemic Respiratory Failure

NCT04395807

Lund University

16 February 2024

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