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Effects of Nutritional Products on Blood Glucose in Subjects With Type 2 Diabetes

Primary Purpose

Diabetes Mellitus, Type 2

Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Nutritional Formula
Usual diet
Diabetes Meal Plan with experimental diabetes-specific nutritional shake, diabetes specific cereal, and diabetes specific snack bars.
Sponsored by
Abbott Nutrition
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes Mellitus, Type 2

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. type 2 diabetes
  2. HbA1c >6.5% and <11.0%
  3. male/non-pregnant, non-lactating female, at least 6 months postpartum
  4. if female of childbearing potential, practicing method of birth control
  5. Body Mass Index > 18.5 kg/m2 and < 43.0 kg/m2.
  6. weight stable for past two months
  7. if on anti-hypertensive, lipid-lowering, thyroid medication or hormone therapy, dosage constant for at least two months

Exclusion Criteria:

  1. uses injected medications (e.g., insulin, exenatide) for glucose control.
  2. history of diabetic ketoacidosis
  3. current infection ; inpatient surgery, or corticosteroid treatment in the last 3 months or antibiotics in the last 3 weeks
  4. active malignancy
  5. states he/she has had a significant cardiovascular event < 12 weeks prior to study entry or history of congestive heart failure in the last 12 months.
  6. end stage organ failure
  7. active metabolic, hepatic, or gastrointestinal disease that may interfere with nutrient absorption, distribution, metabolism, or excretion (such as gastroparesis), excluding diabetes.
  8. chronic, contagious, infectious disease, such as active tuberculosis, Hepatitis B or C, or HIV.
  9. use of herbals, dietary supplements, or medications, other than allowed medications, during past four weeks that could profoundly affect blood glucose.
  10. symptomatic in response to blood collection prior to enrollment into this study.
  11. clotting or bleeding disorders.
  12. non-typical eating pattern
  13. is currently using diabetes-specific nutritional product(s)defined as more than one eating occasion per week.
  14. engages in strenuous exercise five or more times per week.

Sites / Locations

  • Provident Clinical Research
  • Radiant Research

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Experimental

Arm Label

A1

A2

A3

Arm Description

Diabetes Meal Plan with Experimental Diabetes-Specific nutritional shake

Usual diet

Diabetes Meal Plan with Experimental Diabetes-Specific Nutritional Shake, diabetes specific Cereal, and diabetes specific snack bars.

Outcomes

Primary Outcome Measures

Average daily blood glucose level

Secondary Outcome Measures

Percentage of time in specified glucose ranges; Glycemic excursions; Change in plasma glucose, insulin, free fatty acids, triglycerides, 1,5-anhydroglucitol, and fructosamine; Dietary intake variables

Full Information

First Posted
September 12, 2008
Last Updated
April 24, 2009
Sponsor
Abbott Nutrition
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1. Study Identification

Unique Protocol Identification Number
NCT00753181
Brief Title
Effects of Nutritional Products on Blood Glucose in Subjects With Type 2 Diabetes
Official Title
Effects of Nutritional Products on Blood Glucose in Subjects With Type 2 Diabetes
Study Type
Interventional

2. Study Status

Record Verification Date
April 2009
Overall Recruitment Status
Completed
Study Start Date
August 2008 (undefined)
Primary Completion Date
December 2008 (Actual)
Study Completion Date
March 2009 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Abbott Nutrition

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
To evaluate average daily blood glucose in subjects with type 2 diabetes following a Meal Plan including Diabetes-Specific products compared to average daily blood glucose in subjects following their usual diet.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Type 2

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
A1
Arm Type
Experimental
Arm Description
Diabetes Meal Plan with Experimental Diabetes-Specific nutritional shake
Arm Title
A2
Arm Type
Active Comparator
Arm Description
Usual diet
Arm Title
A3
Arm Type
Experimental
Arm Description
Diabetes Meal Plan with Experimental Diabetes-Specific Nutritional Shake, diabetes specific Cereal, and diabetes specific snack bars.
Intervention Type
Other
Intervention Name(s)
Nutritional Formula
Intervention Description
nutritional shake daily
Intervention Type
Other
Intervention Name(s)
Usual diet
Intervention Description
usual dietary habits
Intervention Type
Other
Intervention Name(s)
Diabetes Meal Plan with experimental diabetes-specific nutritional shake, diabetes specific cereal, and diabetes specific snack bars.
Intervention Description
nutritional shake, diabetes specific cereal and diabetes snack bar daily
Primary Outcome Measure Information:
Title
Average daily blood glucose level
Time Frame
11 days
Secondary Outcome Measure Information:
Title
Percentage of time in specified glucose ranges; Glycemic excursions; Change in plasma glucose, insulin, free fatty acids, triglycerides, 1,5-anhydroglucitol, and fructosamine; Dietary intake variables
Time Frame
11 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: type 2 diabetes HbA1c >6.5% and <11.0% male/non-pregnant, non-lactating female, at least 6 months postpartum if female of childbearing potential, practicing method of birth control Body Mass Index > 18.5 kg/m2 and < 43.0 kg/m2. weight stable for past two months if on anti-hypertensive, lipid-lowering, thyroid medication or hormone therapy, dosage constant for at least two months Exclusion Criteria: uses injected medications (e.g., insulin, exenatide) for glucose control. history of diabetic ketoacidosis current infection ; inpatient surgery, or corticosteroid treatment in the last 3 months or antibiotics in the last 3 weeks active malignancy states he/she has had a significant cardiovascular event < 12 weeks prior to study entry or history of congestive heart failure in the last 12 months. end stage organ failure active metabolic, hepatic, or gastrointestinal disease that may interfere with nutrient absorption, distribution, metabolism, or excretion (such as gastroparesis), excluding diabetes. chronic, contagious, infectious disease, such as active tuberculosis, Hepatitis B or C, or HIV. use of herbals, dietary supplements, or medications, other than allowed medications, during past four weeks that could profoundly affect blood glucose. symptomatic in response to blood collection prior to enrollment into this study. clotting or bleeding disorders. non-typical eating pattern is currently using diabetes-specific nutritional product(s)defined as more than one eating occasion per week. engages in strenuous exercise five or more times per week.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vikkie Mustad, PhD
Organizational Affiliation
Abbott Nutrition
Official's Role
Study Director
Facility Information:
Facility Name
Provident Clinical Research
City
Bloomington
State/Province
Indiana
ZIP/Postal Code
47403
Country
United States
Facility Name
Radiant Research
City
Cincinnati
State/Province
Ohio
ZIP/Postal Code
45242
Country
United States

12. IPD Sharing Statement

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Effects of Nutritional Products on Blood Glucose in Subjects With Type 2 Diabetes

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