View Clinical Trial (Medical Research Study)
Bone Microarchitecture in Women With and Without Fracture - NCT01049191-53705B(Clinical Trial 465017)
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Madison |
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State:
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WI |
| Zip Code: |
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53705 |
| Conditions: |
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Osteoporosis - Fracture |
| Purpose: |
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Osteoporosis is a common disorder of compromised bone strength causing 40-50% of women and
~25% of men to sustain fragility fractures during their lifetime. The reduction of bone
strength in osteoporotic people results from loss of bone density and deterioration of bone
quality. Bone quality is a complex amalgamation including macro- and micro-architecture,
mineralization, turnover and damage accumulation. Currently, medications to reduce fracture
risk are prescribed primarily on the basis of bone mineral density (BMD) measurement.
Unfortunately, currently available BMD measurement technologies do not detect the
aforementioned properties of bone quality; as such, less than half of individuals who
sustain osteoporotic fractures are classified as "osteoporotic" by currently available
diagnostic tools. Clearly, measures to enhance identification of those at high fracture
risk are needed. High-resolution magnetic resonance imaging (HR-MRI) technology, such as
that provided by MicroMRI, Inc., has outstanding potential to be such a tool. Therefore,
our long-term goal is to evaluate and optimize the use of HR-MRI in fracture risk
prediction; this pilot work is an essential step in attaining this goal.
This research will investigate 72 postmenopausal women with normal or osteopenic BMD by
dual-energy x-ray absorptiometry (DXA), 36 with prior low-trauma fractures will be compared
with 36 age-, race- and BMD matched women without fracture. We hypothesize that 1.) Women
with fractures will have evidence of microarchitectural deterioration on HR-MRI and 2.)
Newly developed, more rapid MRI sequences designed at the UW will provide similar trabecular
microstructure information more rapidly than the currently used, albeit investigational,
technology produced by MicroMRI, Inc.
Our specific aims are to a) Evaluate differences in MicroMRI parameters of trabecular
microstructure (bone volume fraction, trabecular thickness, surface/curve ratio and erosion
index) between age-, race- and BMD-matched postmenopausal women with and without fracture;
b.) Correlate T2* relaxation time (a rapid indirect MRI measure of trabecular density and
microstructure) with BMD measured by DXA, and microstructural parameters measured by
MicroMRI. As an exploratory aim we will investigate HR-MRI parameters of trabecular
microstructure obtained using a newly developed, rapid MRI sequence referred to as IDEAL-FSE
with parameters obtained using the currently available MicroMRI, Inc. sequence.
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| Study summary: |
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| Criteria: |
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Inclusion Criteria:
- Postmenopausal women volunteers age ≥ 50 years
- normal BMD or osteopenia (T-score > -2.5 at the L1-4 spine, proximal femur and 1/3rd
radius) by DXA.
- sustained a "fragility" fracture of the spine, hip or wrist, defined as a fracture
occurring with everyday activities including a fall from standing height or less.
- Historical radiographic documentation of fracture will be obtained.
- Criteria as defined above without prior fracture, age and bone density matching a
participant in the fracture group
Exclusion Criteria:
- metabolic bone disease
- malignancy
- renal failure
- use of medications which alter bone turnover
- diseases/conditions leading to the non-dominant arm disuse
- contraindications to MRI. |
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If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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July 12, 2010 |
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