Clinical Trials Directory

Trials / Completed

CompletedNCT00723398

Nutritional Supplements and Hormonal Manipulations for Breast Cancer Prevention

Combination of Low Dose Antiestrogens With Omega-3 Fatty Acids for Prevention of Hormone-independent Breast Cancer

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
266 (actual)
Sponsor
Milton S. Hershey Medical Center · Academic / Other
Sex
Female
Age
35 Years – 70 Years
Healthy volunteers
Accepted

Summary

The overall hypothesis is that the combination of a low dose of the antiestrogen Raloxifene with omega-3 fatty acids will exert a synergistic breast cancer chemopreventive effect due to the crosstalk of their downstream cellular effects leading to decreased proliferation and increased apoptosis of premalignant mammary cells. Based on the investigators hypothesis that upregulation of functional estrogen receptors in the premalignant lesions is also responsible for the development of hormone independent tumors, the investigators postulate that the combination of antiestrogens and omega-3 fatty acids will reduce the development of both hormone-dependent and -independent tumors. At present, there are no known interventions able to decrease the development of hormone-independent tumors, which are more prevalent, more aggressive, leading to the patient's demise. In addition, the investigators postulate that this approach will be safe since it will combine a lower and hence a less toxic dose of Raloxifene with the administration of omega-3 fatty acids which are known to have health benefits, i.e., reduction in cardiovascular risk, beyond their possible chemo preventive effect in breast cancer.

Detailed description

The main objectives of this study are to determine the individual and combined effects of Raloxifene and omega-3 fatty acids on surrogate markers of breast cancer development in healthy, postmenopausal women. The primary endpoint will be mammographic density for which the study has been powered. Breast density is a major risk factor for breast cancer and hence it is chosen to evaluate the potential chemopreventive efficacy of our interventions. Secondary endpoints would include markers of oxidative stress, parameters of estrogen metabolism, markers of inflammation, and markers of IGF-I signaling, all of which have been shown in the literature to have an influence on mammary carcinogenesis. Study Population: Healthy, postmenopausal women between the ages of 35-70 years, undergoing yearly mammograms as part of routine screening practice. Method of Identification of Subjects/Samples/Medical Records: Women reporting for yearly mammograms will be considered for this protocol. They will be given first a screening questionnaire to rule out any co-existing medical condition that would predispose them to thromboembolic events.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTLovaza 4gm oralDietary supplement; Take 4 mg oral capsules daily
DRUGRaloxifene 60 Mg Oral Tablet60 mg orally every day for two years
DRUGRaloxifene 30 Mg Oral Tablet30 mg orally daily for two years
DRUGLovaza 4gm & Raloxifene 30mgLovaza 4gm and Raloxifene 30 Mg orally once per day for 2 years

Timeline

Start date
2009-03-01
Primary completion
2015-04-01
Completion
2015-04-01
First posted
2008-07-28
Last updated
2018-11-01
Results posted
2018-11-01

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00723398. Inclusion in this directory is not an endorsement.