Prospective study for prevention of insufficiency fracture after pelvic irradiation with alendronate and vitamin D
Not Applicable
- Conditions
- terine cervical cancer
- Registration Number
- JPRN-UMIN000013114
- Lead Sponsor
- Kobe University Graduate School of Medicine, Division of Radiation Oncology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Female
- Target Recruitment
- 27
Inclusion Criteria
Not provided
Exclusion Criteria
1)Patients with esophageal disorder 2)Patients who cannot sit upright for 30 minuites 3)Patients with a history of allergy to bisphosphonate or vitamin D 4)Patients with hypocalcemia who need treatment 5)Patients with severely impaired renal function (serum creatinine >1.5mg/dL) 6)Patients with severely impaired liver or heart function 7)Patients who were treated with antiosteoporotic medication 8)Patients who are planned to undergo intensity modulated radiation therapy 9)Patients who are considered to be inappropriate by the physician
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method