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Clinical Trials Detail

Phase 0 Study of Normal Postpartum Involution to Identify the Feasibility of a Life Window for Breast Cancer Chemoprevention

Objective
You will be asked to donate a biopsy of your breast, 3 tubes (approximately 2 Tablespoons) of blood and a urine sample.
IRB Protocol Number
12-0769
Principal Investigator(s)
VIRGINIA BORGES

Cancer Trials

  • No Cancer
  • Breast Cancer
Sponsor(s)
UCCC
Contact
EMILY ROZZO at 303-724-0186
or EMILY.ROZZO@UCDENVER.EDU
Eligibility and Other Participant Information
What To Expect : You will be asked to donate a biopsy of your breast, 3 tubes (approximately 2 Tablespoons) of blood and a urine sample. // Women who are pregnant or nursing are eligible and have not been diagnosed with cancer. All study procedures will be performed after you give birth or after you stop nursing.