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NCT06046131Recruiting

Clinical, Genetic and Environmental Determinants of Prostate Cancer Progression.

Source: ClinicalTrials.gov · Last updated 17 Nov 2025

Brief summary (registry, in English)

The course and progression of prostate cancer is highly variable, depending on the individual characteristics, the aggressiveness of the disease at the time of diagnosis as well as the ethno-geographic origins of the individuals. The general objective of the project is to identify the clinical, genetic and environmental determinants (risk factors) of the evolution, progression and complications of the disease according to the treatment options. Identifying modifiable and non-modifiable prognostic determinants of disease progression is a major challenge. This knowledge will help guide treatment choices but also, especially in high-risk populations (high incidence of disease) to better tailor prevention policies and possibly screening .

Status (registry)
Recruiting
Study type
Interventional
Enrollment
3000 (estimated)
First submitted
14 Sept 2023
Start date
28 Feb 2023
Primary completion date
28 Feb 2039
Lead sponsor
Centre Hospitalier Universitaire de la Guadeloupe
NCT number
NCT06046131

What you commit to

  • Study type: Interventional
  • Planned participants: 3000
  • From 28 Feb 2023 to the primary completion date, 28 Feb 2039
  • 2 sites in 2 countries
  • 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.

Other

  • Physical or mental health judjed by the investigator as precluding participation in the research Protected adults (guardianship, curatorship, safeguard of justice).

Who the study is looking for

  • Adult patients with incident case of prostate cancer Patient consulting the University Hospital of Guadeloupe or the University Hospital of Rennes Patient who resides in the departments of Guadeloupe or Martinique or the community of Saint-Martin or in Britany Patient affiliated or beneficiary of the social security signed consent

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

Full criteria on ClinicalTrials.gov

Sites (2)

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

SiteCityCountrySite status
CHU of Rennes
Coordinator of this site? Confirm its status
RennesFranceNot yet recruiting
CHU of Guadeloupe
Coordinator of this site? Confirm its status
Pointe-à-PitreGuadeloupeRecruiting

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