Vitamin D Supplementation in Patients With Diabetes Mellitus Type 2 (DIMENSION)
Primary Purpose
Diabetes Mellitus Type 2, Vitamin D Deficiency
Status
Completed
Phase
Phase 4
Locations
Singapore
Study Type
Interventional
Intervention
Vitamin D supplementation
Placebo Pill
Sponsored by
About this trial
This is an interventional prevention trial for Diabetes Mellitus Type 2 focused on measuring 25(OH)Vitamin D, Diabetes mellitus, Endothelial Function
Eligibility Criteria
Inclusion Criteria:
- Subjects with Type 2 Diabetes Mellitus
- HbA1c : 6.0-10.0%
- Male of female aged 21-80 years
- Stable Diabetes, blood pressure and hyperlipidemia medications (a 25% dose adjustment is allowed) in the last three months
- Baseline serum 25(0H)D concentration <30ng/ml for randomisation
Exclusion Criteria:
- Baseline serum 25(OH)D concentration >30ng/ml
- Baseline HbA1c>10.1%
- Baseline hypercalcemia (Ca>2.58 mmol/L)
- Known case of Primary Hyperparathyroidism
- Known to be on bisphosphonates
- Known to be on Vitamin D supplementation of 1000 units daily or more in the last one year.
- Chronic renal failure with eGFR<30ml/min
- Known to have cirrhosis of the liver or transaminitis with ALT/AST >3X ULN
- Patients with h/o sarcoidosis, renal calculi or any malignancy
- Patients on current treatment for tuberculosis
- Pregnancy and Lactation
- Women of childbearing potential not taking effective contraceptive measures.
- Patients on long term glucocorticoids or anti-retroviral drugs
- Patients on orlistat or other over the counter preparations that claim to block fat absorption.
- A change in the type of medications for hypertension, diabetes mellitus and hyperlipidemia in the last three months
- Patients who have undergone any form of bariatric surgery
- Patients known to have any malabsorption disorders
- Patients known to have osteoporosis or of baseline BMD scan shows osteoporosis as T score <-2.5SD (for randomisation)
Sites / Locations
- Tan Tock Seng Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
Vitamin D supplementation
Placebo pill
Arm Description
Vitamin D3 tablets (cholecalciferol)
Placebo pill
Outcomes
Primary Outcome Measures
Endothelial function as assessed by the reactive hyperemia index and endothelial progenitor cells
Endothelial function will be tested by using the EndoPAT machine which measures the reactive hyperemia index and by estimating the no. of endothelial progenitor cells in the peripheral blood by flow cytometry.
Secondary Outcome Measures
Markers of endothelial cell activation and thrombogenesis
Biomarkers measured include hsCRP, e-selectin,von-willebrand factor(vWF)
No. of circulating endothelial cells and endothelial microparticles
The no. of circulating endothelial cells and endothelial microparticles will be estimated before and after intervention.
Full Information
NCT ID
NCT01741181
First Posted
November 30, 2012
Last Updated
November 17, 2014
Sponsor
Tan Tock Seng Hospital
Collaborators
Duke-NUS Graduate Medical School, National Healthcare Group, Singapore
1. Study Identification
Unique Protocol Identification Number
NCT01741181
Brief Title
Vitamin D Supplementation in Patients With Diabetes Mellitus Type 2
Acronym
DIMENSION
Official Title
Vitamin D Supplementation in Patients With Diabetes Mellitus Type 2 and Low 25(OH)D Concentrations: Does it Help to Improve Endothelial Function-The DIMENSION TRIAL
Study Type
Interventional
2. Study Status
Record Verification Date
November 2014
Overall Recruitment Status
Completed
Study Start Date
September 2012 (undefined)
Primary Completion Date
November 2014 (Actual)
Study Completion Date
November 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Tan Tock Seng Hospital
Collaborators
Duke-NUS Graduate Medical School, National Healthcare Group, Singapore
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Background and Objectives :
The presence of vitamin D deficiency in patients with type 2 diabetes mellitus (T2DM) is associated with an increased risk of cardiovascular disease (CVD). We aim to see whether supplementation of vitamin D in these patients helps to improve the endothelial function (EF) a surrogate marker of CVD risk.
Hypothesis: Vitamin D supplementation in patients with T2DM and low serum 25(OH) D concentrations (<30ng/ml) will improve EF as measured by the Endo-PAT machine by 0.4 units (30% improvement over baseline) and/or will result in a increase of EPCs (CD133+/KDR+) and CD45dim CD34+/KDR.
The investigators will test this hypothesis by comparing 2 groups of T2DM patients randomized to placebo or vitamin D3 for 16 weeks.
Methods:
This is a 16 weeks trial in which 120 T2DM patients will be screened with the aim to recruit 60 T2DM patients with vitamin D deficiency or insufficiency. Out of these 60 patients , 30 patients will be started on vitamin D supplementation and 30 patients will be given a matched placebo. Endothelial function (EF) will be checked before and after supplementation to see a change in EF.
Significance of Project:
If this study shows a significant improvement of EF, it would justify larger scale studies to show that vitamin D supplementation in patients with T2DM mitigates CVD risk and vitamin D supplementation in patients with T2DM and vitamin D deficiency to improve CVD risk.
Detailed Description
Overall Aims: Type 2 Diabetes Mellitus (T2DM) is increasingly more prevalent in Singapore and is a high cardiovascular diseases (CVD) risk factor (1,2). The presence of low serum 25(OH)D concentrations (<30ng/ml) has also been classified as an independent predictor of CVD(3,4) and has been seen to be more prevalent in T2DM (5-7). We aim to see whether replacement with vitamin D in these patients helps to mitigate CVD risk. Since endothelial dysfunction is one of the earliest manifestations of CVD and is a very robust surrogate marker, we aim to measure the endothelial function (EF) before and after vitamin D supplementation to evaluate for beneficial impact on this endpoint.
Specific Aims: Although, there are some small scale studies done with a single high dose replacement of vitamin D2/D3, no studies have been done using regular daily supplementation with vitamin D3 and with measurement of EF using the Endo-PAT machine or measurement of endothelial progenitor cells (EPCs).We are doing this pilot study to see whether replacement with vitamin D results in an improvement of EF as measured using the Endo-PAT and estimation of EPCs and some biomarkers as independent established surrogate markers of CVD risk. The estimation of endothelial progenitor cells has been proposed as a surrogate marker of vascular dysfunction and is known to be reduced in patients with cardiovascular risk factors (8). The no. of circulating endothelial cells (CECs) and endothelial microparticles have been seen to be elevated in patients with cardiovascular risk factors and DM and has also been proposed as a effective surrogate marker. We aim to quantify the no. of endothelial progenitor cells (EPCs) staining positive for CD133+/KDR (kinase insert domain-containing receptor),CD34+/KDR and CD45dim CD34+/KDR , CECs (CD 146+/CD45- ) and EMPs derived from endothelial progenitors (CD45-/CD146+/CD34+/CD117+) and from mature endothelial cells (CD45-/CD146+/CD34+/CD117-).using flow cytometry.
Primary Hypothesis:
Vitamin D supplementation in patients with T2DM and low serum 25(OH) D concentrations (<30ng/ml) will improve EF as measured by the Endo-PAT machine by 0.4 units (30% improvement over baseline) and/or will result in a increase of EPCs (CD133+/KDR+) and CD45dim CD34+/KDR. The investigators will test this hypothesis by comparing 2 groups of T2DM patients randomized to placebo or vitamin D3 for 16 weeks.
Secondary Objectives:
To explore the prevalence of low serum 25(OH) D concentrations (<30ng/ml) in T2DM patients and evaluate the difference in the EF in the two groups. To see whether vitamin D supplementation helps to further improve other parameters such as biomarkers, blood pressure, BMI, urine albumin-to-creatinine ratio (ACR), lipid profile of T2DM patients.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus Type 2, Vitamin D Deficiency
Keywords
25(OH)Vitamin D, Diabetes mellitus, Endothelial Function
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
64 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Vitamin D supplementation
Arm Type
Active Comparator
Arm Description
Vitamin D3 tablets (cholecalciferol)
Arm Title
Placebo pill
Arm Type
Placebo Comparator
Arm Description
Placebo pill
Intervention Type
Drug
Intervention Name(s)
Vitamin D supplementation
Other Intervention Name(s)
Vitamin D3-Cholecalciferol 1000units per tablet.
Intervention Description
Vitamin D3 marketed by oneNine57
Intervention Type
Drug
Intervention Name(s)
Placebo Pill
Other Intervention Name(s)
Placebo
Intervention Description
Placebo pill supplied by oneNine 57 imported to Singapore with approval and import licence from HSA.
Primary Outcome Measure Information:
Title
Endothelial function as assessed by the reactive hyperemia index and endothelial progenitor cells
Description
Endothelial function will be tested by using the EndoPAT machine which measures the reactive hyperemia index and by estimating the no. of endothelial progenitor cells in the peripheral blood by flow cytometry.
Time Frame
16 weeks
Secondary Outcome Measure Information:
Title
Markers of endothelial cell activation and thrombogenesis
Description
Biomarkers measured include hsCRP, e-selectin,von-willebrand factor(vWF)
Time Frame
16 weeks
Title
No. of circulating endothelial cells and endothelial microparticles
Description
The no. of circulating endothelial cells and endothelial microparticles will be estimated before and after intervention.
Time Frame
16-20 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Subjects with Type 2 Diabetes Mellitus
HbA1c : 6.0-10.0%
Male of female aged 21-80 years
Stable Diabetes, blood pressure and hyperlipidemia medications (a 25% dose adjustment is allowed) in the last three months
Baseline serum 25(0H)D concentration <30ng/ml for randomisation
Exclusion Criteria:
Baseline serum 25(OH)D concentration >30ng/ml
Baseline HbA1c>10.1%
Baseline hypercalcemia (Ca>2.58 mmol/L)
Known case of Primary Hyperparathyroidism
Known to be on bisphosphonates
Known to be on Vitamin D supplementation of 1000 units daily or more in the last one year.
Chronic renal failure with eGFR<30ml/min
Known to have cirrhosis of the liver or transaminitis with ALT/AST >3X ULN
Patients with h/o sarcoidosis, renal calculi or any malignancy
Patients on current treatment for tuberculosis
Pregnancy and Lactation
Women of childbearing potential not taking effective contraceptive measures.
Patients on long term glucocorticoids or anti-retroviral drugs
Patients on orlistat or other over the counter preparations that claim to block fat absorption.
A change in the type of medications for hypertension, diabetes mellitus and hyperlipidemia in the last three months
Patients who have undergone any form of bariatric surgery
Patients known to have any malabsorption disorders
Patients known to have osteoporosis or of baseline BMD scan shows osteoporosis as T score <-2.5SD (for randomisation)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rinkoo Dalan, MBBS, FRCP
Organizational Affiliation
Tan Tock Seng Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Tan Tock Seng Hospital
City
Singapore
ZIP/Postal Code
308433
Country
Singapore
12. IPD Sharing Statement
Learn more about this trial
Vitamin D Supplementation in Patients With Diabetes Mellitus Type 2
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