Detection of Aggressive Breast Tumors Using Tc-99m-NC100692

Completed

Conditions studied: Breast Cancer

In brief

The purpose of this study is to compare two types of radioactive drugs to see if they provide the same or different information about any disease that may be present in the participants breast.

Key facts

Study ID

NCT00888589

Run by

Michael O'Connor

People needed

40

Starts

2008-05-01

Expected to finish

2014-02-01

Last updated by the study team

2014-03-27

Who can join

Age: 18 and older, up to 90. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Have a lesion on mammogram, ultrasound or breast MRI that measured < 15 mm in diameter, is considered suggestive or highly suggestive of malignancy according to the Breast Imaging Reporting and Data System Atlas criteria (BIRADS 4b, 4c or 5), and is scheduled for biopsy (needle biopsy and/or surgical biopsy).
• OR
• Have a lesion on mammogram, ultrasound or breast MRI that measured > 15 mm in diameter, is known to be malignant and is scheduled for surgery.
• Patient age > 18 years of age.
• Have a negative pregnancy test on the first day of the study, or must be postmenopausal or surgically sterilized.

You may not qualify if…

• Patients will be excluded if they have a small lesion (< 15 mm) and have undergone prior needle biopsy of the lesion (such biopsy may effectively remove all or part of the lesion and angiogenesis associated with wound healing might confound imaging results with 99mTc-NC100692).
• Patient's pregnancy is not negative on the first day of the study, or the patient is unable to complete the pregnancy test
• Patient is unable to sit on a chair for 40 minutes

Where it is running

• Mayo Clinic — Rochester, Minnesota, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.