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Completed No phase listed Observational Accepts healthy volunteers

Bone Mineral Density in Postmenopausal Women at Increased Risk of Breast Cancer And Who Are Receiving Exemestane on MAP3

ClinicalTrials.gov ID: NCT00688246

Public ClinicalTrials.gov record NCT00688246. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 27, 2026, 3:18 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

The Influence of Five Years of Exemestane on Bone Mineral Density in Postmenopausal Women at Increased Risk of Developing Breast Cancer

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

RATIONALE: Learning about the effect of exemestane on bone mineral density in postmenopausal women at increased risk of breast cancer may help plan treatment, decrease the risk of broken bones, and help patients live more comfortably. PURPOSE: This research study is measuring bone mineral density in postmenopausal women at increased risk of developing breast cancer who are receiving exemestane on clinical trial CAN-NCIC-MAP3.

Study identification

NCT ID
NCT00688246
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
NCIC Clinical Trials Group
Network
Enrollment
238 participants

Conditions and interventions

Eligibility (public fields only)

Age range
35 Years and older
Sex
Female
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 10, 2008 (Actual)
Primary completion
Oct 31, 2011 (Actual)
Completion
Jan 10, 2013 (Actual)
Last update posted
Aug 4, 2023

2008 – 2013

United States locations

U.S. sites
13
U.S. states
12
U.S. cities
12
Facility City State ZIP Site status
Los Angeles Biomedical Research Institute Torrance California 90502 —
The George Washington University Washington D.C. District of Columbia 20037 —
Maine Center for Cancer Medicine and Blood Disorders Scarborough Maine 04074-9308 —
Suburban Hospital Cancer Program Bethesda Maryland 20817 —
Massachusetts General Hospital Boston Massachusetts 02114 —
Dana-Farber Cancer Institute Boston Massachusetts 02115 —
Hutzel Women's Health Specialists Detroit Michigan 48201 —
University of Medicine and Dentistry of New Jersey Newark New Jersey 07107 —
University of Oklahoma Oklahoma City Oklahoma 73104 —
The Memorial Hospital of Rhode Island Pawtucket Rhode Island 02860 —
Fletcher Allen Health Care Burlington Vermont 05401 —
Fred Hutchinson Cancer Research Center Seattle Washington 98109-1024 —
Univ. of Wisconsin Center for Women's Health and Madison Wisconsin 53715 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00688246, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 4, 2023 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00688246 live on ClinicalTrials.gov.

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