OLFADIAG: Demonstrating the Diagnostic Power of an Electronic Nose: Study on Exhaled Air Samples

Sponsor
Nouvelle Clinique Bonnefon (Other)
Overall Status
Terminated
CT.gov ID
NCT03721042
Collaborator
University Hospital, Montpellier (Other)
68
1
1
23.7
2.9

Study Details

Study Description

Brief Summary

The investigators don't know yet how the nose and the brain decode the smells. Scientific studies in neuroscience have shown that people who have tumors may have changes in the smell of secretions. Dogs are extremely efficient at detecting these changes, even before imaging studies. A review of the recent literature shows the different work done on the diagnosis of dogs on human pathologies, especially oncology. It is now known that the smell of exhaled gases is representative of the intestinal biotope and that a large number of pathologies are related to the type of microbial populations that inhabit the intestines.

Copying the olfactory organs could thus be of major interest for the early diagnosis of pathologies. More and more works are interested in the diagnostic power of electronic noses. From a technical point of view, these are nano-sensors that mimic the olfactory receptors from the breath gas of the subjects. They analyze the molecules present and compare them with a database to establish a diagnosis according to a probabilistic algorithm.

The use of exhaled air for the diagnosis of cancerous pathologies has already been the subject of scientific work. A classification using the SVM (support vector machine) method using data from 320 sensors made it possible to differentiate patients with lung cancer from controls in 98.8% of cases. The differential diagnosis of obstructive bronchopneumopathy was also very well done in this same study. Another study shows equally encouraging results, highlighting sensitivities and specificities above 80%.

Condition or Disease Intervention/Treatment Phase
  • Device: olfactory measuring device
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
68 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Demonstrating the Diagnostic Power of an Electronic Nose: Pilot Study on Exhaled Air Samples
Actual Study Start Date :
Oct 11, 2018
Actual Primary Completion Date :
Nov 5, 2019
Actual Study Completion Date :
Oct 1, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: exhaled air

exhaled air analysis of patients

Device: olfactory measuring device
Patients blowing into bags then analysis by olfadiag system

Outcome Measures

Primary Outcome Measures

  1. positive predictive value and negative predictive value [18 months]

    positive predictive value and negative predictive value of the electronic nose

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • The patient must have signed the free and informed consent form or their guardian if applicable. If the state of health of the patient does not allow him to give and sign his consent, it will be sought from the person of trust

  • The patient must be an affiliate or beneficiary of a health insurance plan

  • The patient is at least 18 years old

Exclusion Criteria:
  • The patient participates or has participated within 3 months in another study that may have modified their intestinal biotope

  • The patient is in an exclusion period determined by a previous study

  • The patient is under the protection of justice

  • The patient or guardian or trusted person refuses to sign the consent

  • The patient does not read the French language fluently

  • The patient claims to be pregnant

  • The patient is breastfeeding

Contacts and Locations

Locations

Site City State Country Postal Code
1 Nouvelle Clinique Bonnefon Ales France 34

Sponsors and Collaborators

  • Nouvelle Clinique Bonnefon
  • University Hospital, Montpellier

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Nouvelle Clinique Bonnefon
ClinicalTrials.gov Identifier:
NCT03715855
Other Study ID Numbers:
  • HSM_NCB_2018-1
  • NCT03715855
First Posted:
Oct 26, 2018
Last Update Posted:
Apr 14, 2022
Last Verified:
Apr 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 14, 2022