The Use of Molecular Breast Imaging in the Evaluation of Tumor Response to Neoadjuvant Therapy in Women With Breast Cancer
Completed
Conditions studied: Neoadjuvant Therapy, Chemotherapy, Hormone Replacement Therapy, Breast Cancer
In brief
In patients with breast cancer who undergo neoadjuvant chemotherapy or neoadjuvant hormone therapy molecular breast imaging (MBI) is an accurate test for assessing response rate to neoadjuvant therapy.
Key facts
- Study ID
- NCT01023802
- Run by
- Mayo Clinic
- People needed
- 20
- Starts
- 2009-02-01
- Expected to finish
- 2011-02-01
- Last updated by the study team
- 2013-05-10
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Women with breast cancer scheduled to undergo neoadjuvant chemotherapy therapy or neoadjuvant hormone therapy and who have undergone any breast imaging procedure, and in whom a repeat imaging procedure is planned prior to definite surgery. MRI of the breast for accurate tumor size evaluation is recommended but not necessarily required for study inclusion.
- Are able to return for a 3-5 week follow-up MBI study and for the final MBI study at completion of the neoadjuvant therapy.
- Patient age > 18
You may not qualify if…
- Unable to understand or sign a consent form
- Pregnant or lactating
- Physically unable to sit upright and still for 40 minutes
Where it is running
- Mayo Clinic - Rochester — Rochester, Minnesota, United States
Full record on ClinicalTrials.gov
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