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Clinical Trial Summary

PROSper is a prospective cohort study of 100 women 35-50 years of age with BRCA 1/2 mutations who have elected to either undergo risk reducing salpingo-oophorectomy (RRSO) or nonsurgical management. The investigators will compare the change in cardiovascular health, bone health, sexual function, quality of life, and menopausal symptoms over 3 years of follow-up between women who undergo RRSO (baseline just prior to surgery) and age-matched controls that do not undergo RRSO. The investigators hypothesis is that women who undergo a premature surgical menopause induced by RRSO have worse cardiovascular health and bone health compared with women who do not undergo RRSO.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01948609
Study type Observational
Source University of California, San Francisco
Contact
Status Completed
Phase
Start date July 2014
Completion date December 2021

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