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The Use of an Electronic Nose to Distinguish Between Bacterial and Non-Bacterial Exacerbations of Chronic Obstructive Pulmonary Disease.

An Observational Study on The Use of an Electronic Nose to Distinguish Between Bacterial and Non-Bacterial Exacerbations of Chronic Obstructive Pulmonary Disease.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ANZCTR
Registry ID
ACTRN12611000624987
Acronym
NOSE-COPD
Enrollment
100
Registered
2011-06-20
Start date
2011-01-01
Completion date
Unknown
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

The electronic Nose detects and analyses volatile organic compounds in a gas sample. It has previously been used in the food industry and to detect explosives. By sampling exhaled air in a single breath from a patient, the technology can be used to provide a profile which may define underlying pathology in the airways and lung. In this study we will obtain recordings using the Nose from otherwise well patients with chronic obstructive pulmonary disease (COPD) undergoing pulmonary rehabilitation (n=50) and patients experiencing an acute exacerbation of COPD (n=50). We will compare the Nose signal between these groups, and assess them for the presence or absence of bacterial infection, to see whether there is a nose signal which is characteristic for bacterial infection (which might indicate the need for antibiotic therapy). The aim is to develop bedside technology which is easy to use and provides clinicians with practical information as to whether or not an acute exacerbation is or is not caused by bacterial rather than viral infection. Patients will receive best standard care and the results of the Nose sampling will not alter their standard treatment in any way.

Interventions

No intervention. Exhaled breath sampling during and after Acute Exacerbation of COPD (AECOPD). Collection of exhaled breath via facemask into a reservoir, and subsequent analysis of volatile organic compund profiles by electronic nose. This is a novel 32 sensor device which records a VOC "pattern" which can be used for discrimination of samples. Also characterisation of patients into infected / non-infected groups by use of sputum and blood cultures, nasopharyngeal swab for respiratory virus scr

No intervention. Exhaled breath sampling during and after Acute Exacerbation of COPD (AECOPD). Collection of exhaled breath via facemask into a reservoir, and subsequent analysis of volatile organic compund profiles by electronic nose. This is a novel 32 sensor device which records a VOC "pattern" which can be used for discrimination of samples. Also characterisation of patients into infected / non-infected groups by use of sputum and blood cultures, nasopharyngeal swab for respiratory virus screen by PCR, serology etc. 1-2 years. Also analysis of exhaeled breath by PTR-MS. Exhaled breath samples are taken at exacerbation and again at recovery (approx 6 weeks later) in the patients group, and only once in the control group.

Sponsors

University of Otago
Lead SponsorUniversity

Eligibility

Sex/Gender
All
Age
45 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

Diagnosed COPD

Exclusion criteria

Forced Expiratory Volume in 1 second (FEV1) / Forced Vital Capacity (FVC) percentage (FEV1/FVC) greater than 70% (FEV1) less than 40% predicted Other significant pulmonary disease

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026