Viewing Study NCT00090857


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Study NCT ID: NCT00090857
Status: COMPLETED
Last Update Posted: 2018-03-30
First Post: 2004-09-07
Is NOT Gene Therapy: True
Has Adverse Events: True

Brief Title: Letrozole in Preventing Breast Cancer in Postmenopausal Women
Sponsor: Dana-Farber Cancer Institute
Organization:

Study Overview

Official Title: A Pilot Study of Aromatase Inhibitors for Women at Increased Risk of Breast Cancer Based on Estradiol Levels
Status: COMPLETED
Status Verified Date: 2018-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: WISE
Brief Summary: RATIONALE: Chemoprevention therapy is the use of certain drugs to try to prevent the development or recurrence of cancer. Letrozole may be effective in preventing the development or recurrence of breast cancer in postmenopausal women who are at increased risk of developing breast cancer because of elevated estradiol levels.

PURPOSE: This randomized phase II trial is studying how well letrozole works in preventing breast cancer in postmenopausal women with elevated estradiol levels.
Detailed Description: OBJECTIVES:

Primary

* The primary outcome of the study is the change in bone mineral density following a year on letrozole vs. a year on placebo.

Secondary

* Compare the safety, acceptability, and adherence to letrozole vs placebo in postmenopausal women at increased risk for the development or recurrence of breast cancer based on elevated plasma estradiol levels through evaluation of menopausal symptoms (including hot flushes, weight changes, sexual functioning, and genitourinary effects), blood lipid levels, markers of bone turnover, and multidimensional quality of life.
* Determine the effect of letrozole-induced reduction of plasma estradiol levels on mammographic percent breast density.
* Obtain background information for a future large chemoprevention trial to address the question of whether a reduction in plasma estradiol levels can reduce the risk of breast cancer in postmenopausal women.

OUTLINE: This is a pilot, randomized, double-blind, placebo-controlled, multicenter study. Patients are randomized to 2:1 (experimental treatment: placebo arms).

PROJECTED ACCRUAL: A total of 110 patients (73 for arm I and 37 for arm II) will be accrued for this study.

Study Oversight

Has Oversight DMC: True
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?:

NCT ID Aliases

NCT ID Alias NCT ID View
None NCT00090857 View
None NCT00090857 View
None NCT00090857 View
None NCT00090857 View

Secondary ID Infos

Secondary ID Type Domain Link View
P50CA089393 NIH None https://reporter.nih.gov/quic… View
P30CA006516 NIH None https://reporter.nih.gov/quic… View
DFCI-00024 None None View
UCLA-0210012-02 None None View