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

 


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


Trial Focus

Breast Cancer

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 #

12-0769

Trial Status

OPEN

Principle Investigator

VIRGINIA BORGES

Sponsor

UCCC

Contact

EMILY ROZZO at (303)724-0186 or EMILY.ROZZO@UCDENVER.EDU

Location

University of Colorado Hospital University of Colorado Hospital

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.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.