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A Retrospective Study to Evaluate the Predictability of Abnormal Arterial Blood Gas Measurements Through Novel Observations of Continuous Trends in Electronically Measured Respiratory Rate in a Mixed Cohort of Respiratory Compromised Patients

B

Beaumont Hospital

Status

Unknown

Conditions

COVID-19
Respiratory Failure
Community-acquired Pneumonia
Pulmonary Disease
Pneumonia
COPD

Treatments

Device: RespiraSense

Study type

Observational

Funder types

Other

Identifiers

NCT05384314
RespiraSense ABG investigation

Details and patient eligibility

About

A retrospective study to evaluate the predictability of abnormal arterial blood gas measurements through novel observations of continuous trends in electronically measured respiratory in a mixed cohort of respiratory compromised patients.

Enrollment

322 estimated patients

Sex

All

Ages

18 to 99 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Respiratory condition is the primary admission diagnosis

Exclusion criteria

  • Pregnant patients in their 2nd or 3rd trimester

Trial design

322 participants in 2 patient groups

COPD
Description:
Patients admitted with COPD as the primary admission.
Treatment:
Device: RespiraSense
Respiratory Compromised General
Description:
Patients admitted with Pneumonia, COPD, COVID, to be included
Treatment:
Device: RespiraSense

Trial contacts and locations

1

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Central trial contact

Richard Costello

Data sourced from clinicaltrials.gov

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