Metabolic Adaptation to Diabetes
Primary Purpose
Type 2 Diabetes
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
glucose clamp
glucose clamp
Sponsored by

About this trial
This is an interventional treatment trial for Type 2 Diabetes focused on measuring Type 2 diabetes, intensive therapy
Eligibility Criteria
Inclusion Criteria:
- Healthy male and female subjects aged 30-65 years
- Male and female non-insulin-dependent diabetic patients, sulfonylurea and/or Metformin aged 30-65 years
Exclusion Criteria:
- Prior or current history of poor health
- Abnormal results following screening tests
- Pregnancy
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
1
2
Arm Description
Baseline clamp study before treatment phase.
Final clamp experiment after 6 months intensive therapy.
Outcomes
Primary Outcome Measures
HbA1c
Secondary Outcome Measures
Catecholamines
Full Information
NCT ID
NCT00732862
First Posted
August 8, 2008
Last Updated
December 10, 2014
Sponsor
Vanderbilt University
Collaborators
US Department of Veterans Affairs, Juvenile Diabetes Research Foundation
1. Study Identification
Unique Protocol Identification Number
NCT00732862
Brief Title
Metabolic Adaptation to Diabetes
Official Title
Metabolic Adaptation to Diabetes
Study Type
Interventional
2. Study Status
Record Verification Date
December 2014
Overall Recruitment Status
Completed
Study Start Date
February 1998 (undefined)
Primary Completion Date
March 2000 (Actual)
Study Completion Date
December 2008 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Vanderbilt University
Collaborators
US Department of Veterans Affairs, Juvenile Diabetes Research Foundation
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Hypoglycemia or low blood sugar is a very serious complication that diabetics experience. This is of great concern because there is a lack of available information of how Non Insulin Dependent Diabetic Mellitus patients (NIDDM) defend themselves against a low blood sugar. This is particularly disturbing since NIDDM patients are likely to require intensive treatment, and as a result, the risks of severe hypoglycemia to the NIDDM patient increase. The current proposal aims to provide information on how NIDDM patients can defend themselves against hypoglycemia, thus decreasing their risks for this severe complication.
Detailed Description
There is very little data available on the neuroendocrine response to hypoglycemia in intensively treated (sulfonylurea or insulin) NIDDM patients. The data that are available on the neuroendocrine response to hypoglycemia in NIDDM patients were obtained under conditions following a single IV bolus of insulin or single SQ regular insulin injection. The neuroendocrine response following a large IV bolus of insulin differs greatly from the clinical paradigm of a slow progression into hypoglycemia. Therefore, clinically relevant data cannot be obtained from short experiments involving rapid changes in plasma glucose levels and insulinemia. Furthermore, a comparison between neuroendocrine responses to hypoglycemia in NIDDM and normal man is not available due to the fact that glycemia has never been equally controlled. In short, virtually nothing is known about the neuroendocrine response to hypoglycemia in these subjects. This is of great concern as following the positive outcome of the Kumamato study, large numbers of NIDDM subjects are going to receive intensive therapy with all its altendent risks of severe hypoglycemia. The Kumamato study was a trial in NIDDM patients to determine if intensive therapy reduces tissue complications of diabetes. Similar to the results of the Diabetes control and complications trial in IDDM patients the Kumamato study proved that intensive therapy in NIDDM patients also prevents diabetic tissue complications. Therefore, the goals of this study are 1) to define in greater detail how the body defends itself against hypoglycemia in NIDDM patients and 2) to determine if differing levels of insulin affect hypoglycemic counterregulation in NIDDM patients.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 2 Diabetes
Keywords
Type 2 diabetes, intensive therapy
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
15 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Experimental
Arm Description
Baseline clamp study before treatment phase.
Arm Title
2
Arm Type
Active Comparator
Arm Description
Final clamp experiment after 6 months intensive therapy.
Intervention Type
Procedure
Intervention Name(s)
glucose clamp
Intervention Description
Hyperinsulinemic Hypoglycemic clamp
Intervention Type
Procedure
Intervention Name(s)
glucose clamp
Intervention Description
Hyperinsulinemic Hypoglycemic clamp
Primary Outcome Measure Information:
Title
HbA1c
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Catecholamines
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Healthy male and female subjects aged 30-65 years
Male and female non-insulin-dependent diabetic patients, sulfonylurea and/or Metformin aged 30-65 years
Exclusion Criteria:
Prior or current history of poor health
Abnormal results following screening tests
Pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stephen N Davis, MD
Organizational Affiliation
Vanderbilt University
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
Metabolic Adaptation to Diabetes
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