Vitamin D Deficiency Clinical Trial
Official title:
Effects of Vitamin D Deficiency and Its Replacement on Pulmonary and Endocrine Function in Persons With SCI
Verified date | March 2017 |
Source | James J. Peters Veterans Affairs Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Studies have shown that individuals who have suffered a spinal cord injury are at an increased risk of Vitamin D deficiency compared to able-bodied individuals. It has recently been shown that Vitamin D deficiency is linked to a large number of diseases and conditions, including chronic lung disease, vascular problems, and insulin resistance. If this common nutritional deficiency is proven to be the cause of some of these diseases and conditions in persons with SCI, then it may easily be remedied with a cheap and effective therapeutic approach: vitamin D replacement therapy. Because of the high prevalence of vitamin D deficiency in persons with SCI, this therapy alone or in combination with other treatment options will be expected to significantly improve overall well being in the SCI population, decrease hospitalization rate, and the lower the financial burden of care.
Status | Completed |
Enrollment | 88 |
Est. completion date | December 2016 |
Est. primary completion date | December 2015 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 75 Years |
Eligibility |
Part 1: Screening for Vitamin D Deficiency Inclusion Criteria: - Between the ages of 18 and 75, - Chronic (>1 year) SCI; tetraplegia (C3-8), paraplegia, (T1-6) Exclusion Criteria: - Acute illness - Acute drug or alcohol use - Lack of mental capacity to give informed consent, - Pregnancy, - Currently receiving Vitamin D supplementation. Part 2A: Vitamin D and Pulmonary Function Inclusion Criteria: - Between the ages of 18 and 75, - Chronic SCI (>1 year, C3-T6) - Vitamin D deficiency as defined as a value <20 ng/ml. Exclusion Criteria: - Smoking, active or history of smoking during life time, - Any history of blast injuries to the chest, - Active respiratory disease, - Pregnancy, - Lack of mental capacity to give informed consent. - Recent (within 3 months) respiratory infection. - Receiving medications known to alter airway caliber. - Acute drug or alcohol use, - Currently receiving Vitamin D supplementation > 1000 units/day. Part 2B: Vitamin D, Carbohydrate Metabolism, and Insulin Resistance Inclusion Criteria: - Between the ages of 18 and 75, - Chronic SCI (>1 year, C3-T6) - Vitamin D deficiency as defined as a value <20 ng/ml, - Insulin Resistance (IR), Impaired glucose tolerance (IGT), and/or Diabetes Mellitus (DM). Exclusion Criteria: - Pregnancy, - Problems with the kidneys, - Lack of mental capacity to give informed consent, - Acute drug or alcohol use, - Currently receiving Vitamin D supplementation > 1000 units/day. |
Country | Name | City | State |
---|---|---|---|
United States | James J Peters VA Medical Center | Bronx | New York |
Lead Sponsor | Collaborator |
---|---|
James J. Peters Veterans Affairs Medical Center |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Pulmonary function improvement as measured by inflammation in SCI with vitamin D supplementation. | Pulmonary function change will be measured in vitamin D deficient SCI subjects by biomarkers of inflammation, such as FeNO, pH, and 8-isoprostane, at baseline, 3 months, and 6 months. | Change from baseline at 6 months | |
Other | Impaired glucose tolerance (IGT) improvement in SCI with vitamin D supplementation | Vitamin D deficient SCI subjects with IGT and/or IR will undergo vitamin D replacement therapy. Glucose and insulin levels will be measured at baseline, 3 months, and 6 months. | Change from baseline at 6 months | |
Other | Musculoskeletal pain improvement with vitamin D supplementation | Vitamin D deficient SCI subjects will complete a pain survey at baseline, 3 months, and 6 months to assess musculoskeletal pain and how it may improve with vitamin D supplementation. | Change from baseline at 6 months | |
Primary | Number of SCI participants with vitamin D deficiency | Vitamin D levels will be obtained during screening. | Screening study (1 visit, 2 hours) | |
Secondary | Pulmonary function improvement as measured by PFTs in SCI with increased vitamin D levels | Pulmonary function change will be measured in vitamin D deficient SCI subjects by spirometry and body plethysmography at baseline, 3 months, and 6 months. | Change from baseline at 6 months |
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