Osteoporosis Clinical Trial
Official title:
Low-level Mechanical Vibration, Bone Density, Bone Resorption and Muscular Strength in Ambulant Children Affected by Duchenne Muscular Dystrophy
NCT number | NCT05281120 |
Other study ID # | 02C701 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | November 2006 |
Est. completion date | November 2007 |
Verified date | March 2022 |
Source | Istituto Auxologico Italiano |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Duchenne muscular dystrophy (DMD) is a X-linked recessive disorder due to a mutation of the dystrophin gene (Xp21). Dystrophin is a sarcolemmal protein of skeletal and cardiac muscle, and its absence causes progressive muscle degeneration and substitution with fat and connective tissue. The progressive muscle degeneration leads to loss of autonomous walking before the age of 15 years and death for cardiac and/or respiratory failure. There are no specific treatment for DMD, and the standard of care is now based on long-term corticosteroid (CS) use. The studies on bone mass in DMD are very few, but they agree in reporting the presence of a reduced bone mass and an increased rate of fractures probably due to long-term steroid therapy and disuse-osteopenia. The aim of this study, involving 20 ambulant DMD boys (age 7-10 years) has been the evaluation of the effects of low-level mechanical vibrations on bone in a group of ambulant DMD children for 1 year, with RDA-adjusted dietary calcium intake and 25OH vitamin D supplementation.
Status | Completed |
Enrollment | 20 |
Est. completion date | November 2007 |
Est. primary completion date | May 2007 |
Accepts healthy volunteers | No |
Gender | Male |
Age group | 7 Years to 10 Years |
Eligibility | Inclusion Criteria: - Diagnosis of DMD - Ability to stand up and walk (some balance assistance allowed, but full weight-bearing necessary) - All the children must already be on glucocorticoid therapy for at least 6 months before the start of the study. Exclusion Criteria: - Presence of other diseases interfering with bone density and bone turnover - The inability to regularly use the vibratory platform. |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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Istituto Auxologico Italiano |
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* Note: There are 25 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in bone mineral density at lumbar spine. | Bone mineral density evaluated by DXA. Bone mineral apparent density calculated to correct for bone size (growing subjects). Z-score calculated.
Measurements: baseline and 12 months. |
baseline and 12th month | |
Secondary | Calcium | changes in serum calcium (mg/dL) | baseline and 12th month | |
Secondary | Phosphate | changes in serum phosphate (mg/dL) | baseline and 12th month | |
Secondary | Magnesium | changes in serum magnesium (mg/dL) | baseline and 12th month | |
Secondary | Creatinine | changes in serum creatinine (mg/dL) | baseline and 12th month | |
Secondary | Bone Alkaline Phosphatase | changes in serum bone alkaline phosphatase (µg/L) | baseline and 12th month | |
Secondary | Osteocalcin | changes in serum osteocalcin (µg/L) | baseline and 12th month | |
Secondary | Parathyroid Hormone | changes in serum parathyroid hormone (ng/L) | baseline and 12th month | |
Secondary | 25-OH vitamin D | changes in serum 25-OH vitamin D (µg/L) | baseline and 12th month | |
Secondary | 1,25(OH)2 vitamin D | changes in serum 1,25(OH)2 vitamin D (ng/L) | baseline and 12th month |
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