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NCT Number: NCT06113432

CPAP Therapy Through a Helmet or a Full Face Mask in Patients With Acute Hypoxemic Respiratory Failure: Cross-over Study

Observational and randomized trials have demonstrated the high effectiveness of non-invasive helmet ventilatory support, demonstrating a reduction in intubation rate mortality compared with high-flow and standard oxygen therapy. Some pilot physiological studies have shown physiological benefits of helmets compared to the oronasal mask for non-invasive ventilation. The purpose of the study is to compare markers of patient self-inflicted lung injury (P-SILI), patient's comfort, work of breathing, gas exchange, and hemodynamics in patients with acute hypoxemic respiratory failure (AHRF) during non-invasive ventilation (NIV) in continuous positive pressure (CPAP) mode during an oronasal mask ventilation or a combination of a helmet with high-flow oxygenation as an air flow generator.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

City clinical hospital named after F.I.Inozemtsev, Moscow

Moscow, 105187, Russia

About this study

In December 2019, an outbreak of a novel coronavirus emerged in Wuhan, China and rapidly spread worldwide. The World Health Organization (WHO) declared the outbreak a pandemic on March 11th, 2020. The clinical disease (COVID-19) results in critical illness in about 5% of patients with predominant acute respiratory failure. Observational and randomized trials have demonstrated the high effectiveness of non-invasive helmet ventilatory support, demonstrating a reduction in intubation rate mortality compared with high-flow and standard oxygen therapy. Some pilot physiological studies have shown physiological benefits of helmets compared to the oronasal mask for non-invasive ventilation.

The purpose of the study is to compare markers of patient self-inflicted lung injury (P-SILI) (measuring esophageal pressure, transpulmonary pressure during inspiration and expiration), the patient's work of breathing (assessment of accessory muscles work) patient's comfort by visual-analog scale, gas exchange (by PaO2/FiO2 and Respiration Oxygenation Index (ROX-index), and hemodynamics in patients with acute hypoxemic respiratory failure (AHRF) during non-invasive pulmonary ventilation (NIV) in continuous positive pressure (CPAP) mode during an oronasal mask ventilation or a combination of a helmet with high-flow oxygenation as an air flow generator.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with acute hypoxemic respiratory failure due to community-acquired pneumonia or COVID-19
  • The ratio of the partial pressure of oxygen in arterial blood to the inspiratory fraction of oxygen (PaO2/FiO2) is less than 250 mm Hg while breathing atmospheric air
  • Respiratory rate more than > 25 per minute.
  • Written informed consent

Exclusion criteria

  • Patients who achieve the following target parameters with only low-flow oxygen therapy (flow up to 15 l/min): SpO2 > 93%, the patient does not have a subjective feeling of fatigue, there is no visible work of the auxiliary respiratory muscles of the neck,
  • Unstable hemodynamics (systolic blood pressure <90 mm Hg or mean arterial pressure <65 mm Hg) and/or lactic acidosis (lactate >5 mmol/l and/or clinically diagnosed shock) and/or life-threatening arrhythmia,
  • Metabolic acidosis (pH <7.30);
  • Patients who were in the ICU for less than 24 hours for any reason
  • Primary or secondary lung diseases (exacerbation of chronic obstructive pulmonary disease (COPD), bronchial asthma, interstitial lung diseases, metastatic lung disease)
  • Cardiogenic pulmonary edema,
  • Chronic diseases in the stag e of decompensation with the development of extrapulmonary organ dysfunction (liver cirrhosis, progression of cancer, CHF),
  • Glasgow Coma Scale score <14 points,
  • Swallowing disorders
  • Hypercapnia (PaCO2>45 mmHg),
  • The need for urgent tracheal intubation for any reason,
  • Recent head surgery or anatomy that prevents the placement of a helmet or full face mask on the patient,
  • Pregnancy,
  • Inability to cooperate with staff

Treatment and study plan

Arterial blood gases

Diagnostic Test

Measurement of arterial oxygen and tension and arterial dioxide tension, calculation of arterial partial oxygen tension to inspiratory oxygen fraction (PaO2/FiO2) ratio

Respiratory rate (RR)

Diagnostic Test

Measurement of respiratory rate by waveform analysis using a ventilator

Pulseoximeter

Diagnostic Test

Peripheral capillary oxygen saturation (SpO2) measurement and the ROX-index calculation (SpO2/FiO2/RR)

Assessment of accessory respiratory muscles work

Diagnostic Test

Patrick score calculation. Score: 0. No visible tonic or phasic use of neck muscles. 1. Neck muscles taut but with no respiratory modulation (i.e., tonic activity). 2. Mild respiratory modulation in neck muscle contraction. 3. Moderate phasic activity (no supraclavicular or intercostal indrawing). 4. Vigorous phasic activity with indrawing. 5. Vigorous phasic activity with abdominal paradox.

Esophageal pressure measurement

Diagnostic Test

Esophageal pressure measurement on inspiration and expiration with calculation of delta esophageal pressure, transpulmonary pressure and delta transpulmonary pressure

Discomfort Visual Analog Scale (VAS)

Diagnostic Test

From 1 to 10 points, where 1 point - maximal discomfort, 10 points - minimal discomfort.

Noninvasive blood pressure

Diagnostic Test

Noninvasive blood pressure

Heart rate

Diagnostic Test

Heart rate calculation using electrocardiogram monitoring

Primary outcomes

  1. Inspiratory effort

    Time frame: 40 minutes

    Delta esophageal pressure

  2. Inspiratory delta transpulmonary pressure (stress)

    Time frame: 40 minutes

    Inspiratory delta transpulmonary pressure

  3. Expiratory delta transpulmonary pressure

    Time frame: 40 minutes

    Expiratory delta transpulmonary pressure

Secondary outcomes

  1. Oxygenation

    Time frame: 40 minutes

    PaO2/FiO2 calculation

  2. Respiratory rate

    Time frame: 40 minutes

    Measurement of respiratory rate by waveform analysis using a ventilator

  3. ROX index

    Time frame: 40 minutes

    Peripheral capillary oxygen saturation (SpO2) measurement and the ROX-index calculation (SpO2/FiO2/RR)

  4. Patrick's score

    Time frame: 40 minutes

    Patrick's score measurement, minimum 1point, maximum 5 points, higher score means worse outcome. Score: 0. No visible tonic or phasic use of neck muscles. 1. Neck muscles taut but with no respiratory modulation (i.e., tonic activity). 2. Mild respiratory modulation in neck muscle contraction. 3. Moderate phasic activity (no supraclavicular or intercostal indrawing). 4. Vigorous phasic activity with indrawing. 5. Vigorous phasic activity with abdominal paradox.

  5. Discomfort visual analog scale (VAS)

    Time frame: 40 minutes

    Discomfort VAS score calculation, minimum 1point, maximum 10 points, higher score means better outcome

  6. Noninvasive blood pressure

    Time frame: 40 minutes

    Noninvasive blood pressure

  7. Heart rate

    Time frame: 40 minutes

    Heart rate calculation using electrocardiogram monitoring

Sponsors and collaborators

Lead sponsor

I.M. Sechenov First Moscow State Medical University

Other

Registry information

Official study title

CPAP Therapy Through a Helmet or a Full Face Mask in Patients With Acute Hypoxemic Respiratory Failure: a Comparative, Cross-over, Physiological Study

Important dates

Study start
2023
Primary completion
2024
Study completion
2024
First posted
Nov 2, 2023
Registry last updated
Jun 18, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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