Clinical Trials Directory

Trials / Unknown

UnknownNCT00913016

Assessment of Quality of Life, Bone Density and Safety in Postmenopausal Breast Cancer Patients With Letrozole Therapy

Assessment of Quality of Life, Bone Density and Safety in Postmenopausal Breast Cancer Patients With Letrozole (Femara) as an Early Adjuvant Treatment

Status
Unknown
Phase
Study type
Observational
Enrollment
897 (estimated)
Sponsor
Korean Breast Cancer Study Group · Academic / Other
Sex
Female
Age
45 Years
Healthy volunteers
Not accepted

Summary

To compare the overall QoL (Quality of Life) using Trial Outcome index (TOI) of FACT-B questionnaire for 3 years from baseline.

Detailed description

1. TOI is the sum of the scores from the physical and functional well-being and the breast cancer subscales. 2. To assess incidence of adverse events (including cardiovascular, cerebrovascular, and endocrine, musculoskeletal) in Korean postmenopausal breast cancer patients in early adjuvant setting. 3. To assess the effect of letrozole (Femara) on BMD in early adjuvant setting. 4. To assess the effect of letrozole (Femara) on total cholesterol in early adjuvant setting.

Conditions

Timeline

Start date
2007-06-01
Primary completion
2012-06-01
Completion
2012-06-01
First posted
2009-06-03
Last updated
2010-02-17

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT00913016. Inclusion in this directory is not an endorsement.