A Study to Determine Biopsy Rate in Participants With a First Relapse of Breast Cancer
NCT ID: NCT02761616
Last Updated: 2017-02-01
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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COMPLETED
76 participants
OBSERVATIONAL
2016-06-30
2016-11-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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eBC treated participants
Participants with metastatic disease after previously being treated for eBC were observed for 24 months.
eBC treated participants
No intervention administered in this retrospective observational study.
Interventions
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eBC treated participants
No intervention administered in this retrospective observational study.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
FEMALE
No
Sponsors
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Hoffmann-La Roche
INDUSTRY
Responsible Party
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Principal Investigators
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Clinical Trials
Role: STUDY_DIRECTOR
Hoffmann-La Roche
Locations
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Cemic; Oncologia Clinica
Buenos Aires, , Argentina
Hospital de Morón
Morón, , Argentina
CENICLAR
Rosario, , Argentina
Centro Medico San Roque
San Miguel de Tucumán, , Argentina
Countries
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Other Identifiers
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ML30038
Identifier Type: -
Identifier Source: org_study_id
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