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Trial Summary

Protocol No.TBCRC034
StatusOPEN TO ACCRUAL
Principal InvestigatorLudwig, Kandice
ScopeNational
PhaseNA
Age GroupAdult
TitleThe incidence of Adjacent Synchronous Ipsilateral Infiltrating Carcinoma and/or DCIS in patients diagnosed with Flat Epithelial Atypia (FEA) or Intraductal Papilloma without Atypia (IPWA) by Core Needle Biopsy
DescriptionThis research study is studying a surgical intervention to rule out the presence of cancer in participants that have been diagnosed with flat epithelial atypia (FEA) or intraductal papilloma without atypia (IPWA) by core needle biopsy.
Key EligibilityIn order to be eligible to take part in this trial, patients must meet the following criteria:

  • Women all races and ethnic groups are eligible for this trial. This trial is open to the accrual of women only.
  • Patients must have an imaging abnormality that necessitated a core needle biopsy
For a full list of participation criteria, please visit clinicaltrials.gov.
Applicable Disease SitesBreast Cancer
Participating InstitutionsIU Health North Hospital
  • IU Health North Hospital
IU Health West Hospital
  • IU Health West Hospital
Indiana University (IU)
  • Eskenazi Hospital
  • Indiana University Hospital / IU Simon Cancer Center
Treatment TypeDiagnostic
ContactPhone: (317) 278-5632
Email: iutrials@iu.edu