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NCT05558735Completed

Contribution of Canine Detection in the Diagnostic Strategy of High-risk Prostate Cancer (Prostate-K9-Detect)

Contribution of Canine Detection in the Diagnostic Strategy of High-risk Prostate Cancer

Source: ClinicalTrials.gov · Last updated 11 Aug 2026

Brief summary (registry, in English)

The sense of smell allows both humans and dogs to carry out a chemo-sensory analysis of their environment. Volatile organic compounds enter the nasal cavities and bind to receptors in the nasal mucosa. Neuroepithelium cells perform chemoelectric transduction of olfactory information. The latter is supported by one of the fibers of the olfactory nerve which crosses the cribriform plate of the ethmoid to arrive in the olfactory bulb of the brain. Incorporating this information can lead to behavioral responses. The dog has a sense of smell 100,000 times more sensitive than humans, it is able to detect one particle among 1 trillion. The use of detection dogs involves learning the behavioral response to an olfactory stimulus. Prostate cancer represents 25% of male cancers, it is the second deadliest cancer in France with 10,000 deaths per year. Diagnosis of prostate cancer requires a Prostate Specific Antigen (PSA) blood test and a digital rectal examination. In the event of an abnormality in one of these parameters, a prostate MRI is indicated, supplemented by prostate biopsies in the event of an abnormal MRI. However, one situation remains open to discussion: what should be done when faced with a normal MRI despite an abnormal PSA level or digital rectal examination? In this situation and according to current recommendations, the practitioner has the choice between performing prostate biopsies, i.e. an invasive procedure with a high risk of being negative, and simple monitoring, this time with the risk of missing the diagnosis of prostate cancer. Several studies have shown the effectiveness of dogs in detecting very specific volatile organic compounds. Can the investigators train them to detect the catabolites of prostate tumours?

Status (registry)
Completed
Study type
Observational
Enrollment
183 (actual)
First submitted
15 Sept 2022
Start date
2 Nov 2022
Primary completion date
1 Dec 2023
Lead sponsor
Assistance Publique - Hôpitaux de Paris
NCT number
NCT05558735

What you commit to

  • Study type: Observational
  • Participants enrolled: 183
  • From 2 Nov 2022 to the primary completion date, 1 Dec 2023
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Persons receiving care psychiatric

Other illness

  • Persons whose general condition does not allow to participate in the study

Other

  • Absence of signed informed consent
  • People who do not speak French
  • Protected populations: under guardianship or under curatorship
  • Persons deprived of their liberty by a judicial or administrative decision
  • Absence of affiliation to a pension scheme social Security"

Criteria the registry did not label

  • "Inclusion criteria :
  • Older than 18 years old
  • Requiring the realization of a collection of urine from the framework of their care
  • Requiring a PSA blood test, prostate MRI and prostate biopsies in the framework of their care

Age in the registry: 18 years to - · Sex: Male · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Hôpital Bichat - Claude-Bernard
Coordinator of this site? Confirm its status
ParisFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.