Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
10000 participants
OBSERVATIONAL
2015-02-28
2025-12-31
Brief Summary
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The scientific community will easily have access to clinical and biological informations through a centralized, structured database , leading to optimize patients with breast cancer treatment.
Detailed Description
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Conditions
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Keywords
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Study Design
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PROSPECTIVE
Interventions
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clinical biological database collection
Eligibility Criteria
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Inclusion Criteria
* Histologically confirmed breast cancer of any stage
* Affiliated to a social security system in france
* Who signed the informed consent
Exclusion Criteria
18 Years
FEMALE
No
Sponsors
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Institut Claudius Regaud
OTHER
Responsible Party
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Principal Investigators
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Florence DALENC, MD
Role: PRINCIPAL_INVESTIGATOR
Institut claudius regaud Toulouse ONCOPOLE
Locations
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Institut claudius regaud IUCT ONCOPOLE
Toulouse, , France
Countries
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Central Contacts
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Facility Contacts
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Florence DALENC, MD
Role: primary
Other Identifiers
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15HLSEIN01
Identifier Type: -
Identifier Source: org_study_id