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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01655810
Other study ID # 201102160
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 13, 2012
Est. completion date February 9, 2018

Study information

Verified date June 2020
Source Washington University School of Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

African-Americans have higher rates of cardiovascular disease morbidity and mortality, as well as vitamin D deficiency. Multiple observational studies have demonstrated an increased risk of vitamin D deficiency in African Americans with type 2 diabetes and correlation between cardiovascular disease and vitamin D levels; however, there is a lack of interventional trials exploring this connection. The objective of this proposal is to address the hypothesis that treatment of vitamin D deficiency in African Americans with type 2 diabetes will improve subclinical markers of cardiovascular disease.


Description:

This study will be a double blinded, randomized controlled trial of vitamin D3 supplementation, 4,000 international units per day versus 600 international units per day, for one year to determine the effects on markers of subclinical cardiovascular disease in African Americans with type 2 diabetes and vitamin D deficiency. Outcome assessment will focus on changes in carotid intima-medial thickness (CIMT - ultrasound of the thickness of blood vessels in the neck), as well as markers of systemic inflammation.


Recruitment information / eligibility

Status Completed
Enrollment 86
Est. completion date February 9, 2018
Est. primary completion date February 9, 2018
Accepts healthy volunteers No
Gender All
Age group 50 Years to 70 Years
Eligibility Inclusion Criteria:

- African Americans of both genders

- Age 50-70 years

- Type 2 diabetes (A1C < 9.0%), on stable therapy with oral medications, insulin, or a combination

- 25(OH)D level < 20 ng/ml

- BP < 140/90 mmHg; LDL < 140 mg/dl

Exclusion Criteria:

- Pregnancy

- Cardiovascular disease

- Stage 3 or worse chronic kidney disease

- High urine or serum calcium or history of recurrent kidney stones

- Unstable medical conditions or major systemic diseases such as malignancy

Study Design


Intervention

Dietary Supplement:
Vitamin D3
Multivitamin containing cholecalciferol 4000 units orally daily
Vitamin D3
Multivitamin containing cholecalciferol 600 units orally daily
Calcium carbonate
500 mg orally twice daily

Locations

Country Name City State
United States Washington University Saint Louis Missouri

Sponsors (2)

Lead Sponsor Collaborator
Washington University School of Medicine American Diabetes Association

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change from baseline in carotid intima-medial thickness 0, 6, and 12 months
Secondary Change from baseline in systemic inflammatory markers 0, 6, and 12 months
Secondary Serum calcium 0, 1, 3, 6, 9, and 12 months
Secondary Urinary Calcium 0, 1, 3, 6, 9, and 12 months
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