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EUClinicalTrials.govClinical trialNot applicableActive, not recruiting

Investigation of Tumour Spectrum of Germline Mutations in Breast and Ovarian Cancer Genes.

Official record

Identifier
NCT03246841
Recruiting locations

country

France
Interventions studied
Genetic testing
Lead sponsor
UNICANCER
Target enrolment
7274 participants
Study type
INTERVENTIONAL
Phase
Not applicable
Status
Active, not recruiting
First posted
Aug 11, 2017
Last updated on the registry
Jul 31, 2026
Age
18 Years – 75 Years
Sex
ALL
Study contact
No public contact is listed on the official record.
Eligibility criteria

Reproduced verbatim from the official record. Eligibility is decided by the study team, never by this page.

Inclusion criteria:

Index case eligibility:

Any person with an indication for a BRCA1/BRCA2 gene analysis and who has been offered TUMOSPEC panel screening.

Age ≥18 years.

Family member eligibility:

Family members will be eligible if the mutation identified in the Index Case is considered deleterious.

Any family member to the first and second decree or a cousin of the Index Case. Family members from both sides of the family will be invited to take part.

Age ≥18 years.

Exclusion Criteria:

People deprived of their civil liberties or who are under judicial protection or guardianship.

Patients unable to answer the questionnaire for social or psychological reasons.

Children of the index cases, of any age.

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