A Study of Biological, Genetic, and Constitutional Factors and Non-invasive Monitoring to Assess Personal Cancer Risks

Recruiting Observational Study
Breast Cancer Colo-rectal Cancer Ovarian Cancer Melanoma (Skin Cancer) Non-Small Cell Lung Cancer (MeSH Term: Carcinoma, Non-Small-Cell Lung)
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
850 (estimated)
Sponsor
Fondazione del Piemonte per l'Oncologia · Other
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About This Trial
The PRO-ACTIVE study aims to develop a clinical-translational program in the field of cancer prevention in all its phases (primary, secondary, and tertiary) to intervene before the clinical and radiological manifestation of the disease. It starts with risk prediction and leads to early diagnosis of the disease or recurrence in the subclinical phase. The PRO-ACTIVE study includes the following act…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Age \>18 years; * Patients with breast cancer, including patients who meet the AIOM criteria for eligibility for BRCA testing and patients with lobular breast cancer; * Patients with radically resected colon cancer, including patients with stage III colon cancer and vascular i…
Contacts

Vanesa Gregorc, MD

+390119933915

vanesa.gregorc@ircc.it

CONTACT