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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00839696
Other study ID # CC07104
Secondary ID 2008-1013A538500
Status Completed
Phase
First received
Last updated
Start date July 2008
Est. completion date April 2010

Study information

Verified date December 2014
Source University of Wisconsin, Madison
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Mammographic density is sensitive to estorgen exposure and constitutes a strong intermediate maker of breast cancer risk. We hypothesize that women with higher serum xenoestrogen levels will have greater mammographic density.


Recruitment information / eligibility

Status Completed
Enrollment 270
Est. completion date April 2010
Est. primary completion date June 2009
Accepts healthy volunteers No
Gender Female
Age group 55 Years to 70 Years
Eligibility Inclusion Criteria:

- 55-70 years of age, Post menopausal

Exclusion Criteria:

- If they have ever used hormone replacment therapy or have ever used Tamoxifen or Raloxifene, Diag. with breast cancer have had breast implants or have had a mastectomy/

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States University of Wisconsin Hospital Madison Wisconsin

Sponsors (2)

Lead Sponsor Collaborator
University of Wisconsin, Madison United States Department of Defense

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Characterize the distribution of total xenoestrogen burden and identify important source of xenoestrogen exposure among a clinic-based sample of postmenopausal women. 1 year
Secondary Evaluate the association of total xenoestorgen exposure with mammographic density. 1 year
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