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Effects of Micronutrient (Chromium) Supplementation on Diabetes

Primary Purpose

Diabetes Mellitus, Type 1

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
chromium niacinate
placebo
Sponsored by
Louisiana State University Health Sciences Center Shreveport
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes Mellitus, Type 1 focused on measuring Diabetes Mellitus, Juvenile Onset, Cardiovascular Diseases, Hyperglycemia, Hyperketonemia

Eligibility Criteria

8 Years - 21 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Clinical diagnosis of Type 1 diabetes mellitus
  • Participants between the ages of 8 and 21

Exclusion Criteria:

  • Subjects with sickle cell disease, renal or liver disease
  • Serum positive pregnancy test or breastfeeding
  • Participants unwilling/unable to take supplements in pill form
  • Participants taking prescription medication or supplements

Sites / Locations

  • Louisiana State University Health Sciences Center in Shreveport

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

placebo

chromium niacinate

Arm Description

Placebo supplementation in pill form for 3 months following randomization after a placebo run-in period.

Chromium niacinate supplementation (200ug or 500ug/day) in pill form for 3 months following randomization after a placebo run-in period

Outcomes

Primary Outcome Measures

Blood Glucose Level
Measuring levels of glycemia (fasting glucose) in blood of patients in the placebo group and the chromium supplement group.
Blood Glucose Levels
Measuring levels of glycemia (HbA1c) in blood patients in the placebo group and the chromium supplement group.

Secondary Outcome Measures

Lipid Levels
Measuring levels of TG (triglycerides), LDL and HDL-cholesterol in blood of patients in the placebo group and the chromium supplement group.
Blood Levels of Cytokines/Inflammatory Biomarkers
Measuring levels of reactive oxygen species (ROS) in blood of patients in the placebo group and chromium supplement group.
Blood Levels of Cytokines/Inflammatory Biomarkers
Measuring levels of Interleukin-6 (IL-6) in blood of patients in the placebo group and chromium supplement group.
Blood Levels of Cytokines/Inflammatory Biomarkers
Measuring levels of C reactive protein (CRP) in blood of patients in the placebo group and chromium supplement group.
Blood Levels of Cytokines/Inflammatory Biomarkers
Measuring levels of Leptin in blood of patients in the placebo group and chromium supplement group.

Full Information

First Posted
October 16, 2012
Last Updated
June 29, 2022
Sponsor
Louisiana State University Health Sciences Center Shreveport
Collaborators
National Institutes of Health (NIH), National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
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1. Study Identification

Unique Protocol Identification Number
NCT01709123
Brief Title
Effects of Micronutrient (Chromium) Supplementation on Diabetes
Official Title
Ketosis, Vascular Inflammation, and Its Therapy (Chromium Supplementation) in Diabetic Patients
Study Type
Interventional

2. Study Status

Record Verification Date
June 2022
Overall Recruitment Status
Completed
Study Start Date
August 2007 (undefined)
Primary Completion Date
September 2013 (Actual)
Study Completion Date
September 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Louisiana State University Health Sciences Center Shreveport
Collaborators
National Institutes of Health (NIH), National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
6-8% of USA population has diabetes. Intensive blood glucose control dramatically reduces the devastating complications that result from poorly controlled diabetes. However, for many patients, achievement of tight glucose control is difficult with current regimens. Trivalent chromium, the form found in foods and dietary supplements, is believed to be safe. Our preliminary studies have reported that chromium supplementation inhibits the increase in pro-inflammatory cytokines (tumor necrosis factor-alpha and interleukin-6; TNF-alpha and IL-6) secretion levels caused by high glucose levels in cultured monocytic cells. Similarly, animal studies have shown that chromium niacinate supplementation lowered blood levels of glycemia and pro-inflammatory cytokines in streptozotocin-treated diabetic rats. Cytokines are proteins that are secreted by monocytes and other cells in response to various stimuli, such as infection. Some of the cytokines are known to regulate insulin sensitivity and elevated level of these cytokines in blood may accelerate clogging of arteries. Thus, chromium supplementation may increase insulin sensitivity and glycemic control in diabetic patients, and may prevent the development of cardiovascular disease in diabetic patients. Given the enormous public health cost of diabetes, the prospect of being able to use a relatively low-cost dietary supplement, such as chromium, as an adjuvant therapy to help in achieving normal blood glucose level merits further study. We will examine the effects of placebo and chromium niacinate supplementation on the fasting glucose, cholesterol, triglycerides, and markers of vascular disease in blood of diabetic patients. We will determine these above parameters at baseline and after the 1, 2 and 3 months of supplementation in diabetic patients. The long-term objective is to explore the efficacy of chromium as an adjuvant treatment for better glycemic control, prevent the development of cardiovascular disease (CVD), and improve the life expectancy in diabetic population. Chromium supplements are widely used by the public and are available in many stores, such as Wal-mart, Walgreens, and many other food and drug stores. Chromium is an essential trace metal and micronutrient present in wide variety of vegetables. Niacin is a vitamin B6, an essential vitamin for our body. This study plans to use chromium niacinate, a complex of chromium and niacin. Chromium niacinate is considered a nutrient.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Type 1
Keywords
Diabetes Mellitus, Juvenile Onset, Cardiovascular Diseases, Hyperglycemia, Hyperketonemia

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
62 (Actual)

8. Arms, Groups, and Interventions

Arm Title
placebo
Arm Type
Placebo Comparator
Arm Description
Placebo supplementation in pill form for 3 months following randomization after a placebo run-in period.
Arm Title
chromium niacinate
Arm Type
Experimental
Arm Description
Chromium niacinate supplementation (200ug or 500ug/day) in pill form for 3 months following randomization after a placebo run-in period
Intervention Type
Drug
Intervention Name(s)
chromium niacinate
Intervention Description
200ug or 500ug supplementation in pill form
Intervention Type
Drug
Intervention Name(s)
placebo
Intervention Description
Placebo pill for chromium niacinate
Primary Outcome Measure Information:
Title
Blood Glucose Level
Description
Measuring levels of glycemia (fasting glucose) in blood of patients in the placebo group and the chromium supplement group.
Time Frame
Assessed for 16 weeks with 5 measurements. (0 weeks, 4 weeks, 8 weeks, 12 weeks, 16 weeks), 16 weeks reported.
Title
Blood Glucose Levels
Description
Measuring levels of glycemia (HbA1c) in blood patients in the placebo group and the chromium supplement group.
Time Frame
Assessed for 16 weeks with five measurements. (0 weeks, 4 weeks, 8 weeks, 12 weeks, 16 weeks). 16 weeks reported.
Secondary Outcome Measure Information:
Title
Lipid Levels
Description
Measuring levels of TG (triglycerides), LDL and HDL-cholesterol in blood of patients in the placebo group and the chromium supplement group.
Time Frame
Assessed for 16 weeks with 5 measurements. (0 weeks, 4 weeks, 8 weeks, 12 weeks, 16 weeks), 16 weeks reported.
Title
Blood Levels of Cytokines/Inflammatory Biomarkers
Description
Measuring levels of reactive oxygen species (ROS) in blood of patients in the placebo group and chromium supplement group.
Time Frame
Assessed for 16 weeks with 5 measurements. (0 weeks, 4 weeks, 8 weeks, 12 weeks, 16 weeks), 16 weeks reported.
Title
Blood Levels of Cytokines/Inflammatory Biomarkers
Description
Measuring levels of Interleukin-6 (IL-6) in blood of patients in the placebo group and chromium supplement group.
Time Frame
Assessed for 16 weeks with 5 measurements. (0 weeks, 4 weeks, 8 weeks, 12 weeks, 16 weeks), 16 weeks reported.
Title
Blood Levels of Cytokines/Inflammatory Biomarkers
Description
Measuring levels of C reactive protein (CRP) in blood of patients in the placebo group and chromium supplement group.
Time Frame
Assessed for 16 weeks with 5 measurements. (0 weeks, 4 weeks, 8 weeks, 12 weeks, 16 weeks), 16 weeks reported.
Title
Blood Levels of Cytokines/Inflammatory Biomarkers
Description
Measuring levels of Leptin in blood of patients in the placebo group and chromium supplement group.
Time Frame
Assessed for 16 weeks with 5 measurements. (0 weeks, 4 weeks, 8 weeks, 12 weeks, 16 weeks), 16 weeks reported.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
8 Years
Maximum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Clinical diagnosis of Type 1 diabetes mellitus Participants between the ages of 8 and 21 Exclusion Criteria: Subjects with sickle cell disease, renal or liver disease Serum positive pregnancy test or breastfeeding Participants unwilling/unable to take supplements in pill form Participants taking prescription medication or supplements
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sushil K Jain, Ph.D.
Organizational Affiliation
Louisiana State University Health Sciences Center in Shreveport
Official's Role
Principal Investigator
Facility Information:
Facility Name
Louisiana State University Health Sciences Center in Shreveport
City
Shreveport
State/Province
Louisiana
ZIP/Postal Code
71130
Country
United States

12. IPD Sharing Statement

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Effects of Micronutrient (Chromium) Supplementation on Diabetes

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