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A Study to Assess the Effects of DPP-4 Inhibition on Insulin Sensitivity in Type 2 Diabetes

Primary Purpose

Diabetes Mellitus, Type 2

Status
Completed
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Vildagliptin
Sponsored by
Novartis
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes Mellitus, Type 2 focused on measuring Vildagliptin, Type 2 diabetes, Insulin sensitivity, Insulin action

Eligibility Criteria

21 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Diagnosed with type 2 diabetes at least 3 months prior to screening Blood glucose criteria must be met On stable dose of metformin therapy BMI less than or equal to 39 Exclusion Criteria: Type 1 diabetes, diabetes resulting from pancreatic injury or secondary forms of diabetes Treatment with thiazolidinediones or use of insulin within the previous 3 months Significant illness within 2 weeks prior to dosing High fasting triglycerides as defined by the protocol Other protocol-defined inclusion/exclusion criteria may apply

Sites / Locations

    Outcomes

    Primary Outcome Measures

    Effect on insulin sensitivity at 6 weeks

    Secondary Outcome Measures

    Lipolysis rate after 6 weeks of treatment
    Plasma free fatty acid concentration after 6 weeks of treatment
    Hepatic glucose production after 6 weeks of treatment
    Glucose disposal after 6 weeks of treatment
    Gluconeogenesis rate after 6 weeks of treatment

    Full Information

    First Posted
    July 11, 2006
    Last Updated
    May 4, 2012
    Sponsor
    Novartis
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00351546
    Brief Title
    A Study to Assess the Effects of DPP-4 Inhibition on Insulin Sensitivity in Type 2 Diabetes
    Official Title
    A Study to Assess the Effects of DPP-4 Inhibition on Insulin Sensitivity in Type 2 Diabetes
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    May 2012
    Overall Recruitment Status
    Completed
    Study Start Date
    February 2005 (undefined)
    Primary Completion Date
    November 2005 (Actual)
    Study Completion Date
    December 2005 (Actual)

    3. Sponsor/Collaborators

    Name of the Sponsor
    Novartis

    4. Oversight

    5. Study Description

    Brief Summary
    Type 2 diabetes results when the body does not produce enough insulin and/or is unable to properly use the insulin it makes (insulin resistance). This study was undertaken to assess the effects of vildagliptin on insulin sensitivity in people with type 2 diabetes.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Diabetes Mellitus, Type 2
    Keywords
    Vildagliptin, Type 2 diabetes, Insulin sensitivity, Insulin action

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 3
    Interventional Study Model
    Crossover Assignment
    Masking
    Double
    Allocation
    Randomized
    Enrollment
    12 (Actual)

    8. Arms, Groups, and Interventions

    Intervention Type
    Drug
    Intervention Name(s)
    Vildagliptin
    Primary Outcome Measure Information:
    Title
    Effect on insulin sensitivity at 6 weeks
    Secondary Outcome Measure Information:
    Title
    Lipolysis rate after 6 weeks of treatment
    Title
    Plasma free fatty acid concentration after 6 weeks of treatment
    Title
    Hepatic glucose production after 6 weeks of treatment
    Title
    Glucose disposal after 6 weeks of treatment
    Title
    Gluconeogenesis rate after 6 weeks of treatment

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    21 Years
    Maximum Age & Unit of Time
    65 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Diagnosed with type 2 diabetes at least 3 months prior to screening Blood glucose criteria must be met On stable dose of metformin therapy BMI less than or equal to 39 Exclusion Criteria: Type 1 diabetes, diabetes resulting from pancreatic injury or secondary forms of diabetes Treatment with thiazolidinediones or use of insulin within the previous 3 months Significant illness within 2 weeks prior to dosing High fasting triglycerides as defined by the protocol Other protocol-defined inclusion/exclusion criteria may apply
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    David Kelley, MD
    Organizational Affiliation
    University of Pittsburgh
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Learn more about this trial

    A Study to Assess the Effects of DPP-4 Inhibition on Insulin Sensitivity in Type 2 Diabetes

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