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Early Insulin Treatment in Patients With Latent Autoimmune Diabetes

Primary Purpose

Diabetes, Autoimmune, Diabetes Mellitus, Adult-Onset

Status
Completed
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Insulin
Sponsored by
Lund University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes, Autoimmune

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • >18 yrs
  • Positive for pancreatic autoantibodies

Exclusion Criteria:

  • <18 yrs
  • Significant concomitant diseases
  • Not able to follow protocol

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    No Intervention

    Arm Label

    Insulin treatment

    Conventional treatment

    Arm Description

    Insulin given as soon as possible after diagnosis

    Diet, oral hypoglycemic agents and insulin first when clinically needed

    Outcomes

    Primary Outcome Measures

    Glucagon stimulated C-peptide
    Glucagon stimulated C-peptide is measured at diagnosis and annually for three years. Basal values will be compared to values obtained after 36 months.

    Secondary Outcome Measures

    Full Information

    First Posted
    April 8, 2010
    Last Updated
    April 22, 2010
    Sponsor
    Lund University Hospital
    Collaborators
    Landstinget Kronoberg, Sweden
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    1. Study Identification

    Unique Protocol Identification Number
    NCT01109927
    Brief Title
    Early Insulin Treatment in Patients With Latent Autoimmune Diabetes
    Official Title
    Early Insulin Treatment in Patients With Latent Autoimmune Diabetes (LADA)
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    February 1995
    Overall Recruitment Status
    Completed
    Study Start Date
    February 1995 (undefined)
    Primary Completion Date
    April 2002 (Actual)
    Study Completion Date
    May 2005 (Actual)

    3. Sponsor/Collaborators

    Name of the Sponsor
    Lund University Hospital
    Collaborators
    Landstinget Kronoberg, Sweden

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Among adult patients diagnosed with type 2 diabetes, about 6% have autoantibodies directed against the insulin producing beta cells in the pancreas. These patients have a progressive beta cell destruction and most of them will be insulin dependent within 3-5 yrs. Patients with this latent autoimmune diabetes in adults (LADA) have a considerable remaining beta cell mass at diagnosis, and are suitable for evaluating new therapies for autoimmune diabetes Animal studies in diabetes prone mice have demonstrated potential positive effects of early insulin treatment, with a lower incidence of diabetes or a delay before diagnosis. The aim of this study was to investigate the effect of early insulin treatment of LADA patients, in respect to residual beta-cell function and metabolic control, compared to a group who were conventionally treated with diet and/or oral hypoglycaemic agents (OHA) and insulin not before it was clinically needed.
    Detailed Description
    All adult newly diagnosed diabetic patients in the certain areas are screened for pancreatic antibodies. Patients clinically classified as Type 2, not insulin requiring at diagnosis and positive for at least one autoantibody are eligible for inclusion. After randomisation to insulin treatment or diet and/or OHA, the patients are followed up with fasting C-peptide every third month. A glucagon test is performed, and stimulated C-peptide and HbA1c, + clinical data and body weight are recorded at baseline and after 12, 24 and 36 months. The final outcome of the study is C-peptide, and change in C-peptide compared to baseline level, and HbA1c, after 36 months.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Diabetes, Autoimmune, Diabetes Mellitus, Adult-Onset

    7. Study Design

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

    8. Arms, Groups, and Interventions

    Arm Title
    Insulin treatment
    Arm Type
    Experimental
    Arm Description
    Insulin given as soon as possible after diagnosis
    Arm Title
    Conventional treatment
    Arm Type
    No Intervention
    Arm Description
    Diet, oral hypoglycemic agents and insulin first when clinically needed
    Intervention Type
    Drug
    Intervention Name(s)
    Insulin
    Intervention Description
    Insulin treatment in accordance to glucose values
    Primary Outcome Measure Information:
    Title
    Glucagon stimulated C-peptide
    Description
    Glucagon stimulated C-peptide is measured at diagnosis and annually for three years. Basal values will be compared to values obtained after 36 months.
    Time Frame
    36 months after entering the study

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    90 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: >18 yrs Positive for pancreatic autoantibodies Exclusion Criteria: <18 yrs Significant concomitant diseases Not able to follow protocol

    12. IPD Sharing Statement

    Learn more about this trial

    Early Insulin Treatment in Patients With Latent Autoimmune Diabetes

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