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Dynamic Magnetic Resonance (MR) Study in Evaluating the Vertebral Bone Marrow Perfusion and Its Related Research
This study is currently recruiting participants.
Verified by National Taiwan University Hospital, August 2005
First Received: September 12, 2005   Last Updated: February 28, 2006   History of Changes
Sponsored by: National Taiwan University Hospital
Information provided by: National Taiwan University Hospital
ClinicalTrials.gov Identifier: NCT00172224
  Purpose

The etiology and pathogenesis of osteoporosis has been extensively discussed. The relationship between bone blood circulation and the formation of bony trabeculae has been less understood. There is plenty of indirect evidence highly suggestive of the correlation between these two factors, such as: the number of blood vessels in the per unit area of the bone marrow was decreased in the osteoporotic bone, indicating the possible role of a microvascular defect in the pathogenesis of osteoporosis. Furthermore, the bone mineral density in severe arteriosclerotic patients was lower than in the less affected subjects. In a large scale epidemiologic study, diminished bone mineral density was strongly associated with increased deaths from stroke. Osteopenia was also associated with an increased risk of stroke. These reports highly suggest the effect of ischemia on bone metabolism and make the investigators more interested in further investigation.

A dynamic contrast-enhanced magnetic resonance (MR) study was used recently in evaluating the blood perfusion of bone tumors. This method also has a strong correlation with the microsphere blood flow measurements. The investigator (T.F. Shih) used the dynamic MR in her recent two researches:

  1. To differentiate benign versus malignant spinal compression fractures.
  2. To evaluate the blood perfusion of non-fractured, normal-appearing vertebral bodies and find its significant correlation with aging and sex.

The alterations of bone marrow perfusion are synchronous with the changes of bone mineral density. Thus, based on the investigators' previous research work, they propose to further explore the relationship between bone marrow perfusion and bone mineral density in different age groups.


Condition Phase
Osteoporosis
Fractures, Compression
Phase III

MedlinePlus related topics: Fractures Minerals Osteoporosis
U.S. FDA Resources
Study Type: Observational
Study Design: Natural History, Cross-Sectional, Defined Population, Prospective Study
Official Title: Dynamic MR Study in Evaluating the Vertebral Bone Marrow Perfusion and Its Related Research

Further study details as provided by National Taiwan University Hospital:

Estimated Enrollment: 100
Study Start Date: August 2002
Detailed Description:

The etiology and pathogenesis of osteoporosis has been extensively discussed. The relationship between bone blood circulation and the formation of bony trabeculae has been less understood. There is plenty of indirect evidence highly suggestive of the correlation between these two factors, such as: the number of blood vessels in the per unit area of the bone marrow was decreased in the osteoporotic bone, indicating the possible role of a microvascular defect in the pathogenesis of osteoporosis. Furthermore, the bone mineral density in severe arteriosclerotic patients was lower than in the less affected subjects. In a large scale epidemiologic study, diminished bone mineral density was strongly associated with increased deaths from stroke. Osteopenia was also associated with an increased risk of stroke. These reports highly suggest the effect of ischemia on bone metabolism and make the investigators more interested in further investigation.

A dynamic contrast-enhanced magnetic resonance (MR) study was used recently in evaluating the blood perfusion of bone tumors. This method also has a strong correlation with the microsphere blood flow measurements. The investigator (T.F. Shih) used the dynamic MR in her recent two researches:

  1. To differentiate benign versus malignant spinal compression fractures.
  2. To evaluate the blood perfusion of non-fractured, normal-appearing vertebral bodies and find its significant correlation with aging and sex.

The alterations of bone marrow perfusion are synchronous with the changes of bone mineral density. Thus, based on the investigators' previous research work, they propose to further explore the relationship between bone marrow perfusion and bone mineral density in different age groups.

  Eligibility

Ages Eligible for Study:   20 Years to 80 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Normal subjects
  • Elder subjects with osteoporosis

Exclusion Criteria:

  • History of malignancy or infection
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00172224

Contacts
Contact: Tiffany Ting-Fang Shih, M.D. 886-2-23123456 ext 6993 ttfshih@ha.mc.ntu.edu.tw

Locations
Taiwan
Tiffany Ting-Fang Shih Recruiting
Taipei, Taiwan
Contact: Tiffany Ting-Fang Shih, MD     886-2-23123456 ext 6993     ttfshih@ha.mc.ntu.edu.tw    
Contact: Tiffany Ting-Fang Shih, MD     886-2-23123456 ext 6993     ttfshih@ha.mc.ntu.edu.tw    
Principal Investigator: Tiffany Ting-Fang Shih, MD            
Sponsors and Collaborators
National Taiwan University Hospital
Investigators
Principal Investigator: Tiffany Ting-Fang Shih, M.D. Department of Medical Image, National Taiwan University Hospital
  More Information

No publications provided

Study ID Numbers: 32244, NSC 91-2314-B-002-395, NSC 92-2314-B-002-172
Study First Received: September 12, 2005
Last Updated: February 28, 2006
ClinicalTrials.gov Identifier: NCT00172224     History of Changes
Health Authority: Taiwan: Department of Health

Keywords provided by National Taiwan University Hospital:
osteoporosis
compression fracture
bone marrow perfusion
MR spectroscopy
hormone therapy

Study placed in the following topic categories:
Fractures, Compression
Musculoskeletal Diseases
Fractures, Bone
Wounds and Injuries
Disorders of Environmental Origin
Osteoporosis
Bone Diseases, Metabolic
Hormones
Bone Diseases

Additional relevant MeSH terms:
Fractures, Compression
Musculoskeletal Diseases
Fractures, Bone
Wounds and Injuries
Disorders of Environmental Origin
Osteoporosis
Bone Diseases, Metabolic
Bone Diseases

ClinicalTrials.gov processed this record on May 07, 2009