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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01684735
Other study ID # B322201213618
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 2012
Est. completion date December 2014

Study information

Verified date September 2012
Source Universitaire Ziekenhuizen KU Leuven
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Evaluation of the response to chemotherapy in breast cancer patients by the use of Diffusion-weighted magnetic resonance imaging of the breast before the start of chemotherapy, after one and 3 cycles of therapy and at the end of the therapy.


Recruitment information / eligibility

Status Completed
Enrollment 45
Est. completion date December 2014
Est. primary completion date December 2014
Accepts healthy volunteers No
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria: - core biopsy with diagnosis of breast cancer - start of neo-adjuvant chemotherapy Exclusion Criteria: - magnetic resonance imaging incompatibility

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Belgium University Hospitals Leuven Leuven

Sponsors (1)

Lead Sponsor Collaborator
Universitaire Ziekenhuizen KU Leuven

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Response to chemotherapy outcome is the results of pathology after chemotherapy and surgery. Data will be collected for a period of 1 year. 1 year
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