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Non-Invasive Monitoring of Respiratory Function in Spontaneously Breathing Patients With COVID-19 Infection

Mass General Brigham logo

Mass General Brigham

Status

Terminated

Conditions

COVID-19
Ventilatory Failure
Respiratory Failure
ARDS, Human
Pneumonia

Treatments

Device: AirGo Respiratory Monitor

Study type

Observational

Funder types

Other

Identifiers

NCT04356443
2020P000881

Details and patient eligibility

About

This study uses the AirGo band to monitor changes in tidal ventilation in spontaneously breathing patients with COVID-19 associated respiratory failure. It aims to recognize patterns of ventilation associated with worsening respiratory failure in this patient population. If successful, this study will lead to the development of new robust methods for real-time, continuous monitoring of respiratory function in patients with respiratory failure. In turn, such monitoring methods may enable improvements in the medical management of respiratory failure and timing of interventions.

Enrollment

25 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Admitted to the hospital
  • ≥ 18 years of age
  • Clinically suspected or confirmed COVID-19 infection
  • Spontaneously breathing
  • For patients not on supplemental oxygen at their location of residence prior to hospital admission, need for supplemental O2 to maintain SpO2 >=92%
  • For patients on supplemental O2 at their location of residence prior to hospital admission, an increase in requirement of supplemental oxygen from baseline

Exclusion criteria

  • Intubated patients
  • Pregnant women
  • Moribund patients
  • Patients who are on comfort measures (CMO)

Trial contacts and locations

1

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Central trial contact

Jeanine Wiener-Kronish, MD; Omar Hyder, MD, MS

Data sourced from clinicaltrials.gov

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