Collecting data on patients with a breast cancer who undergo or do not undergo magnetic resonance imaging (MRI) before surgery
- Conditions
- Breast cancerCancerMalignant neoplasm of breast
- Registration Number
- ISRCTN41143178
- Lead Sponsor
- EIBIR, gemeinnützige Gmbh zur Förderung der Erforschung der biomedizinischen Bildgebung
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Female
- Target Recruitment
- 7000
Women from 18 to 80 years of age with a newly diagnosed needle-biopsy proven first breast cancer
1. Pregnancy
2. Previous history of non-breast cancer at any site
3. Previous history of breast cancer (invasive or DCIS)
4. Women candidates to neoadjuvant chemotherapy
5. Women with evidence of distant metastases at the time of breast MRI
6. Women with absolute contraindications to MRI or to gadolinium-based contrast materials according to international guidelines or local regulations (including eGFR <30 ml/min*1.73 m2)
7. Women who received any contrast material prior to breast MRI examination or are scheduled to receive any contrast material within 24 hour afterwards
8. Mental disability precluding informed consent to participate
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method