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Kansas City, Kansas 66160


Purpose:

To determine the efficacy of soy/isoflavone supplementation on hot flashes in men who are being treated with luteinizing hormone-releasing hormone (LHRH) agonist therapy for control of advanced prostate cancer


Study summary:

Literature has shown that low dose estrogens can control hot flashes in men on androgen deprivation but with a high risk of thromboembolic events. Soy derivatives that contain isoflavones, a type of phytoestrogen, have been evaluated in peri-menopausal women as a possible safer alternative to synthetic estrogens but there has not been a similar study performed on their effect in men on androgen deprivation therapy for prostate cancer.


Criteria:

Inclusion Criteria: - Histologically proven adenocarcinoma of prostate with treatment of prostate cancer (radical prostatectomy, radiation therapy, etc.) - had biochemical/clinical relapse and started on antiandrogens - have documented history of hot flashes Exclusion Criteria: - History of MI, DVT, CVA - peanut allergy - untreated hypothyroidism - must be off other medical treatment for hot flashes for 2 weeks before enrollment in this study


NCT ID:

NCT00594620


Primary Contact:

Principal Investigator
Jeffrey M. Holzbeierlein, MD
University of Kansas


Backup Contact:

N/A


Location Contact:

Kansas City, Kansas 66160
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: January 18, 2018

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