Phase
Condition
N/ATreatment
Injection of contrast enhancing agent Imeron for B-CT investigation
Injection of contrast enhancing agent Gadovist for MRI investigation
Clinical Study ID
Ages > 18 Female Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Sex: female
Age: at least 18 years
Inconclusive findings in conventional imaging or preoperative staging or evaluationof therapy response in the neoadjuvant chemotherapy setting or imaging of the breastafter breast-conserving therapy or finding the cause of hemorrhagic nipple dischargeor prosthesis imaging or screening of women with hereditary or familial increasedrisk for the development of breast cancer or axillary lymph node metastasissuspected to originate from breast tissue
Persons able and willing to understand and sign informed consent form
Exclusion
Exclusion Criteria:
Known pregnancy or breastfeeding
Presence of BRCA1 or BRCA2 allele
Insufficient renal function (MDRD)
Dysfunction of the thyroid gland (TSH degradation)
Known allergy or intolerance against iodine-containing contrast enhancing agents orMRI contrast enhancing agents
Patients with paramagnetic or magnetic material inside the breast, claustrophobia
Study Design
Study Description
Connect with a study center
DRZ Die Radiologen
Regensburg, Bavaria 93059
GermanyActive - Recruiting
Radiologisches Institut Universitätsklinikum Erlangen
Erlangen, 91054
GermanyActive - Recruiting
Stichting Martini Ziekenhuis
Groningen, 9728 NT
NetherlandsActive - Recruiting
Leiden University Medical Centre
Leiden, 2333 ZA
NetherlandsActive - Recruiting
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