Texture Analysis for Postmenopausal Osteoporosis
Completed · Not applicable
Conditions studied: Osteoporosis, Osteopenia
In brief
The purpose of this study is to determine if a new test for osteoporosis can be useful in monitoring treatment. We are studying a new method for examining the quality of bone by an experimental method of computerized analysis of radiographic images (x-ray pictures) of the heel.
Key facts
- Study ID
- NCT00145977
- Run by
- University of Chicago
- People needed
- 36
- Starts
- 2001-07-01
- Expected to finish
- 2009-12-01
- Last updated by the study team
- 2018-09-11
Who can join
Age: 59 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- The study will enroll 40 postmenopausal women with a T score < -2 either at the lumbar spine or the femoral neck: 20 who decide to begin anti-resorptive therapy (treated group), and 20 women who decline such therapy (control group). We will attempt to match the patients and the controls for T score (within 0.3) and age (within 5 years).
- All study participants will be:
- at least 3 years past the last menstrual period,
- not on HRT, Raloxifene or calcitonin for at least 6 months.
You may not qualify if…
- All study participants will not be on bisphosphonates during the previous 12 months.
- Women with secondary causes of osteoporosis will be excluded.
Where it is running
- The University of Chicago — Chicago, Illinois, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.