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Effect of Escalating Oral Vitamin D Replacement on HOMA-IR in Vitamin D Deficient Type 2 Diabetics

Primary Purpose

Vitamin D Deficiency, Insulin Resistance, Diabetes Mellitus, Type 2

Status
Completed
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
oral vitamin D
Sponsored by
King Edward Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Vitamin D Deficiency focused on measuring Vitamin D, T2DM, Insulin Resistance

Eligibility Criteria

25 Years - 50 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Both genders
  2. Age 25 to 50 years as type 2 diabetes usually diagnosed in this age range.
  3. Patients having Type 2 Diabetes Mellitus
  4. Taking oral antidiabetic medicines
  5. Serum 25(OH) vitamin D levels below 20ng/ml having no clinical symptoms of vitamin D deficiency.
  6. HOMA-IR > 2.5

Exclusion Criteria:

  1. Patients having evidence of liver dysfunction and chronic renal insufficiency because it will alter the metabolism of cholecalciferol.
  2. Patients having parathyroid dysfunction diagnosed on the basis of blood tests as replacement of vitamin D in these patients is very complex.
  3. Patients having gastrointestinal surgeries that will alter the absorption of cholecalciferol diagnosed from detailed clinical history and clinical examination.
  4. Patients having clinical features of gastroparesis diagnosed on the basis of clinical history as it can alter the absorption of vitamin D.
  5. Patients having erratic control of diabetes requiring multiple hospital admissions for diabetic emergencies.
  6. Pregnant and lactating mothers.

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Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    No Intervention

    Arm Label

    vitamin D

    Conventional

    Arm Description

    vitamin D arm will receive oral vitamin D in escalating dosage.

    This arm will receive conventional treatment only.

    Outcomes

    Primary Outcome Measures

    Homeostatic Model Assessment of Insulin Resistance
    insulin resistance reduction to <2.5

    Secondary Outcome Measures

    Glycated Hemoglobin (HbA1C)
    Reduction by 0.5%

    Full Information

    First Posted
    September 7, 2015
    Last Updated
    December 1, 2019
    Sponsor
    King Edward Medical University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04183257
    Brief Title
    Effect of Escalating Oral Vitamin D Replacement on HOMA-IR in Vitamin D Deficient Type 2 Diabetics
    Official Title
    Effect of Escalating Oral Vitamin D Replacement on HOMA-IR in Vitamin D Deficient Type 2 Diabetics
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    December 2019
    Overall Recruitment Status
    Completed
    Study Start Date
    September 30, 2016 (Actual)
    Primary Completion Date
    April 30, 2017 (Actual)
    Study Completion Date
    July 30, 2017 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    King Edward Medical University

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    In addition to its effect on maintaining calcium homeostasis and mineralization of bone, vitamin D has been linked to play a pivotal role in different medical conditions including type 2 diabetes mellitus. Vitamin D plays a major role in both insulin secretion and decreasing the insulin resistance hence has a major impact on glucose tolerance. This study is designed to determine the non-skeletal effects of vitamin D in improving the glucose tolerance in type 2 diabetic patients by decreasing the insulin resistance
    Detailed Description
    Pakistan stands at seventh spot amongst the world having patients suffering from Type 2 Diabetes Mellitus (T2DM) with the prevalence of approximately 6.9 million in 2007. Among the risk factors for the development of T2DM, there is a growing evidence that deficiency of vitamin D is an independent risk factor for its development and poor glycemic control. Vitamin D plays a significant role not only in secretion of insulin from the beta cells of pancreas but it also helps in decreasing the insulin resistance at the level of target cells. Vitamin D has received an enormous attention recently. A report from Australia indicated 1 in 3 Australians are Vitamin D deficient. Reports from Pakistan have also demonstrated Vitamin D deficiency. The study conducted by Haroon Khan et al had 562 (76.2%) females while 175 (23.8%) were males. Mean age of respondents was 36.3 years (age range 15-75 years. Females had significantly lower mean Vitamin D levels (56.2%) compared to males (15.3%). 25(OH) Vitamin D is the circulating form of vitamin D which is measurable in the blood. Vitamin D insufficiency has been defined as serum 25-hydroxyvitamin D (25(OH) D) levels below 30 ng/mL and it is common among patients with T2DM. Many studies have revealed that Vitamin D3 (calcitriol) has a role in the synthesis and the secretion of insulin by receptor mediated molecular mechanisms. Moreover Vitamin D functions are not limited to skeletal health benefits and may extend to preservation of insulin secretion and insulin sensitivity. Studies have revealed the association between vitamin D deficiency and changes in blood glucose and insulin levels as well as sensitivity of the target tissues to insulin .Cross-sectional data provide some evidence that circulating 25-hydroxyvitamin D (25(OH) D) is inversely associated with insulin resistance, although direct measurements of insulin sensitivity are required for confirmation. Available prospective studies support a protective influence of high 25(OH) D concentrations on type 2 diabetes mellitus risk. Vitamin D receptor gene polymorphisms and vitamin D interactions with the insulin like growth factor system may further influence glucose homeostasis. The ambiguity of optimal vitamin D dosing regimens and optimal therapeutic concentrations of serum 25(OH) D limit available intervention studies. A study found no improvement in glucose tolerance following the administration of two vitamin D doses with an interval of 2 weeks to thirty-seven non-diabetic, vitamin D-deficient adults. Another study reported a randomised, controlled trial of vitamin D3, three fortnightly doses of 120 000 IU or placebo, in centrally obese Indian men. The subjects were not necessarily insulin resistant, but there was some improvement in postprandial insulin sensitivity following supplementation. A recent systematic review and meta-analysis on the role of vitamin D and calcium in type 2 diabetes conclude that 'there appears to be a relationship' but due to the paucity of data, an understanding of the mechanisms is incomplete. This study has a novelty in the dosage and the frequency of administration of vitamin D which has not been studied yet. This study will enable to determine the impact of vitamin D replacement on insulin resistance in vitamin D deficient Type 2 diabetic patients and to find any correlation of serum levels of 25 hydroxyvitamin D levels with the degree of insulin resistance.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Vitamin D Deficiency, Insulin Resistance, Diabetes Mellitus, Type 2
    Keywords
    Vitamin D, T2DM, Insulin Resistance

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 4
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    106 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    vitamin D
    Arm Type
    Experimental
    Arm Description
    vitamin D arm will receive oral vitamin D in escalating dosage.
    Arm Title
    Conventional
    Arm Type
    No Intervention
    Arm Description
    This arm will receive conventional treatment only.
    Intervention Type
    Drug
    Intervention Name(s)
    oral vitamin D
    Other Intervention Name(s)
    oral vitamin D 400IU
    Intervention Description
    oral Vitamin D 400IU will be given and will be escalated every 2 weeks.
    Primary Outcome Measure Information:
    Title
    Homeostatic Model Assessment of Insulin Resistance
    Description
    insulin resistance reduction to <2.5
    Time Frame
    3 months
    Secondary Outcome Measure Information:
    Title
    Glycated Hemoglobin (HbA1C)
    Description
    Reduction by 0.5%
    Time Frame
    3 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    25 Years
    Maximum Age & Unit of Time
    50 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Both genders Age 25 to 50 years as type 2 diabetes usually diagnosed in this age range. Patients having Type 2 Diabetes Mellitus Taking oral antidiabetic medicines Serum 25(OH) vitamin D levels below 20ng/ml having no clinical symptoms of vitamin D deficiency. HOMA-IR > 2.5 Exclusion Criteria: Patients having evidence of liver dysfunction and chronic renal insufficiency because it will alter the metabolism of cholecalciferol. Patients having parathyroid dysfunction diagnosed on the basis of blood tests as replacement of vitamin D in these patients is very complex. Patients having gastrointestinal surgeries that will alter the absorption of cholecalciferol diagnosed from detailed clinical history and clinical examination. Patients having clinical features of gastroparesis diagnosed on the basis of clinical history as it can alter the absorption of vitamin D. Patients having erratic control of diabetes requiring multiple hospital admissions for diabetic emergencies. Pregnant and lactating mothers. -

    12. IPD Sharing Statement

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