New breathing monitor could help doctors spot lung trouble faster
NCT ID NCT05661019
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether a device called MYOTRACE, which measures how hard a person's breathing muscles are working, can help doctors assess patients with respiratory diseases. 56 adults with conditions like COPD or asthma were included. The goal was to see if the device's readings matched a lung specialist's evaluation.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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56 people
The number who actually took part.
- Started
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May 2024
- Finished
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Jan 2025
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
During recruitment of the patients, all patients admitted to the general ward who are having a respiratory disease or condition and satisfy the inclusion criteria will be eligible, including patients returning to general ward from ICU admission.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age 18+, fluent knowledge of English or German. * Group A: Obstructive ventilatory disorders (conditions resulting in an increased load on the respiratory muscle pump due to hyperinflation ± pronounced hypoxaemia) * Acute exacerbation of COPD (pronounced hypoxia OR acute or acute on chronic hypercapnic respiratory failure) * Exacerbation of asthma bronchiale * Exacerbation of non-CF-bronchiectasis (infectious) * Infectious exacerbation of lung disease in cystic fibrosis * Group B: Conditions with an increase in NRD due to an impairment in gas exchange (particularly die to diffusion limitation and/or ventilation-perfusion-mismatch * Exacerbation of an interstitial lung disease (e.g. Idiopathic pulmonary fibrosis (IPF), Non Specific Interstitial Pneumonia (NSIP), Connective tissue disease- associated interstitial lung disease CTD-ILD) * Worsening of pulmonary arterial hypertension World Health Organisation (WHO) group 1 (e.g. due decompensated heart failure) * Acute pulmonary embolism * Pneumonia (resulting in hypoxaemia) Exclusion Criteria: * Obesity hypoventilation syndrome (rationale: NRD decreased) * Obesity WHO III with Body Mass Index (BMI) \> 40 kg/m2 (rationale: surface EMG signal quality low) * Hypercapnic respiratory failure due to hypoventilation of central origin, e.g. opiate-induced, Congenital central hypoventilation syndrome, post stroke (rationale: central respiratory control affected) * Neuromuscular disease affecting respiratory muscles, e.g. motor neurone disease, muscular dystrophy type Duchenne etc. (rationale: EMG signal quality etc. different) * Decompensated heart failure with atrial fibrillation (rationale: central breathing disturbance common) * Patients on chronic opioid therapy (e.g. chronic pain, methadone etc.) (rationale: reduced NRD) * Self reported pregnancy
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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University Hospital Zürich
Zurich, 8091, Switzerland
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