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A prospective study of bone mineral density changes in patients during perioperative chemotherapy for breast cancer

Not Applicable
Recruiting
Conditions
Breast cancer
Registration Number
JPRN-UMIN000053265
Lead Sponsor
Hyogo Prefectural Harima Himeji General Medical Center
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
50
Inclusion Criteria

Not provided

Exclusion Criteria

1) The patients for whom regular bone density testing is not possible 2) THe patients younger than 20 years of age 3) The patients diagnosed with osteoporosis by bone density test 4) The patients using drugs for osteoporosis 5) The patients who are regularly using steroids 6) The patients who judged a study doctor to be inappropriate as subjects

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Rate of decrease in bone mineral density after 4 courses of chemotherapy
Secondary Outcome Measures
NameTimeMethod
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