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Breath Analysis to Diagnose Lung Cancer (CATOCOV)

U

University Hospital, Lille

Status

Completed

Conditions

Lung Cancer

Treatments

Device: Collection of volatile organic compounds during exhalation

Study type

Interventional

Funder types

Other

Identifiers

NCT03250390
2017-A00932-51 (Other Identifier)
2017_05
PHRCI_2016 (Other Identifier)

Details and patient eligibility

About

Determination of volatile organic compounds to discriminate patients with lung cancer from healthy smokers and non-smokers healthy subjects.

Enrollment

1,500 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients with histologically proven lung cancer

Controls:

  • healthy smoker or non-smoker subjects
  • without respiratory diseases excepted chronic obstructive pulmonary disease.

Exclusion criteria

  • history of cancer other than lung cancer within 5 years before inclusion
  • oral or facial malformation
  • incomprehension of maneuvers for the collection

Trial design

Primary purpose

Diagnostic

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

1,500 participants in 2 patient groups

patients
Experimental group
Description:
Patients with bronchopulmonary cancer who have not yet received therapeutic treatment.
Treatment:
Device: Collection of volatile organic compounds during exhalation
controls
Active Comparator group
Description:
The controls consisted of 2 groups: smokers and non-smokers.
Treatment:
Device: Collection of volatile organic compounds during exhalation

Trial contacts and locations

7

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Central trial contact

Sébastien Hulo, MD

Data sourced from clinicaltrials.gov

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