Search Allelic Imbalance of Expression of BRCA Genes in Hereditary Risk of Breast and/or Ovarian Cancer

NCT ID: NCT01333748

Last Updated: 2012-07-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

PHASE2

Total Enrollment

530 participants

Study Classification

INTERVENTIONAL

Study Start Date

2010-04-30

Study Completion Date

2012-06-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The purpose of this study is to determine proportion of patients presented a search allelic imbalance of expression of genes BRCA 1 and 2 in population with hereditary breast and/or ovarian cancer risk and negative for deletion mutation BRCA 1 and 2 genes

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Hereditary Breast and Ovarian Cancer Syndrome

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

breast cancer ovarian cancer BRCA 1 and BRCA 2

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

patients group

Patients with ovarian and/or breast cancer

Group Type EXPERIMENTAL

blood collection

Intervention Type GENETIC

blood collection for research quantification of allelic expression in the gene BRCA1.

control population

control population without history of breast and/or ovarian cancer

Group Type OTHER

blood collection

Intervention Type GENETIC

blood collection for research quantification of allelic expression in the gene BRCA1.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

blood collection

blood collection for research quantification of allelic expression in the gene BRCA1.

Intervention Type GENETIC

blood collection

blood collection for research quantification of allelic expression in the gene BRCA1.

Intervention Type GENETIC

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

For patients

* Women with breast cancer and / or ovarian cancer meet criteria suggestive of a hereditary predisposition
* Deleterious mutation of BRCA1 and BRCA2 sought and not highlighted
* Age ≥ 18 years
* Agreeing to participate in the study (a collection of signed informed consent)

For control population

* Women with no history of breast and / or ovarian cancer and no family history of breast and / or ovarian cancer among family members on the 1st and 2nd degree before age 50 for breast cancer and before 60 years for ovarian cancer
* Agreeing to participate in the study (a collection of signed informed consent)

Exclusion Criteria

For patients:

* Patients with a known deleterious mutation in BRCA1 and BRCA2
* Patients do not meet criteria suggestive of a hereditary predisposition
* Persons deprived of liberty or under guardianship (including guardianship)

For control population:

* Males
* Personal or family history of breast and / or ovarian cancer (breast or ovarian cancer in their family experienced 1st and 2nd degree before age 50 for breast cancer before age 60 for cancer ovarian)
* Persons deprived of liberty or under guardianship (including guardianship)
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Centre Francois Baclesse

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Centre François BACLESSE

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Agnès HARDOUIN, MD

Role: PRINCIPAL_INVESTIGATOR

Centre François Baclesse

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Dr Pascaline BERTHET

Caen, Caen, France

Site Status

Centre Eugène MARQUIS

Rennes, Rennes, France

Site Status

Centre Hospitalier

Cherbourg, , France

Site Status

CHU

Rennes, , France

Site Status

Centre Henri BECQUEREL

Rouen, , France

Site Status

CHU

Rouen, , France

Site Status

Countries

Review the countries where the study has at least one active or historical site.

France

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

2009-A00833-54

Identifier Type: REGISTRY

Identifier Source: secondary_id

EXSAL

Identifier Type: -

Identifier Source: org_study_id