fREEDOM: REsonance for Early Detection Of Breast Cancer Metastases
NCT ID: NCT06328465
Last Updated: 2026-01-06
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
NA
145 participants
INTERVENTIONAL
2019-11-22
2028-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
DIAGNOSTIC
NONE
Study Groups
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DWB-MRI
Surveillance with diffusion whole body MRI
Diffusion whole body MRI
Diffusion whole body MRI protocol, consisting of sagittal T1-weighted and T2-weighted sequences on the whole spine, axial T1 weighted, T2-weighted and diffusion-weighted images from head to mid-thigh, performed on a 1.5 T scanner.
Interventions
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Diffusion whole body MRI
Diffusion whole body MRI protocol, consisting of sagittal T1-weighted and T2-weighted sequences on the whole spine, axial T1 weighted, T2-weighted and diffusion-weighted images from head to mid-thigh, performed on a 1.5 T scanner.
Eligibility Criteria
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Inclusion Criteria
* No evidence of distant metastases at baseline perioperative radiological staging (DWB-MRI, total body Computed Tomography (CT) or Positron Emission Tomography (PET/CT) must be performed +/- 1 month from surgery)
* No relevant comorbidities
* Eastern Cooperative Oncology Group (ECOG) performance status 0
* Geographically accessible for follow up
* Ability to understand and the willingness to sign a written informed consent document
Exclusion Criteria
* Relative contraindications that include situations in which the innocuousness of the examination is not documented with certainty that therefore do not recommend the execution, except for serious indications related to the patient's clinical need
* Older age (\>75 years)
* Previous or concomitant other malignancy except basal or squamous cell carcinoma of the skin or adequately treated in situ carcinoma of the cervix
* Uncontrolled intercurrent illness including symptomatic congestive heart failure, unstable angina pectoris, or psychiatric illness/social situations that would limit compliance with study requirements
18 Years
75 Years
ALL
No
Sponsors
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European Institute of Oncology
OTHER
Responsible Party
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Principal Investigators
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Monica Iorfida, MD
Role: PRINCIPAL_INVESTIGATOR
European Institute of Oncology
Locations
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European Institute of Oncology
Milan, , Italy
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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IEO 1108
Identifier Type: OTHER
Identifier Source: secondary_id
UID 1743
Identifier Type: -
Identifier Source: org_study_id
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