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Treatment of Latent Autoimmune Diabetes of the Adult (LADA)

Primary Purpose

Diabetes

Status
Completed
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
metformin+ NPH insulin
metformin + sitagliptin +/- repaglinide
Sponsored by
Norwegian University of Science and Technology
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes focused on measuring Latent autoimmune diabetes, adults, Beta cell rest, Insulin secretion

Eligibility Criteria

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

Inclusion Criteria:

  • Diabetes diagnosed during 0-3 years before entering the study.
  • Age > or equal to 30 years < or equal to 75 years
  • anti-GAD positivity
  • fasting C-peptide > or equal to 0,3 ng/ml
  • no need for insulin treatment by clinical judgement for at least 3 months following the diagnosis of diabetes.
  • HbA1c > 15 % above the upper limit of normal

Exclusion Criteria:

  • Renal insufficiency (plasma creatinine > 150 mol/L)
  • Severe retinopathy (proliferative or pre-proliferative)
  • Severe cardiac disease (NYHA III-IV)
  • Chronic severe illness judged by the investigator
  • Females of reproductive age who wish to become pregnant during the study

Sites / Locations

  • Valdemar Grill

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Metformin + NPH Insulin

Metformin + sitagliptin +/-repaglinid

Arm Description

Patients are treated with metformin during the run-in period (3 months) and also after randomization. By randomization insulin treatment will be added in the form of injections of NPH insulin in the evenings.

Patients are treated with metformin during the run-in period (3 months) and also after randomization. By randomization sitagliptin tablets will be added.If HbA1c after 6 months of treatment is > 10 % above the upper limit of normal,then treatment with repaglinide tablets tree times daily at mealtimes will be added.

Outcomes

Primary Outcome Measures

insulin secretion
insulin secretion measured by fasting and glucagon-stimulated C-peptide

Secondary Outcome Measures

glycemic control
glycemic control (HbA1c)

Full Information

First Posted
June 8, 2010
Last Updated
January 8, 2020
Sponsor
Norwegian University of Science and Technology
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1. Study Identification

Unique Protocol Identification Number
NCT01140438
Brief Title
Treatment of Latent Autoimmune Diabetes of the Adult
Acronym
LADA
Official Title
Is "Beta Cell Rest" by Insulin Treatment Beneficial Compared to State-of-the Art Enhancers of Insulin Secretion in Preserving Beta Cell Function in Subjects With Latent Autoimmune Diabetes of the Adult (LADA)?
Study Type
Interventional

2. Study Status

Record Verification Date
January 2020
Overall Recruitment Status
Completed
Study Start Date
March 2009 (Actual)
Primary Completion Date
November 2018 (Actual)
Study Completion Date
November 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Norwegian University of Science and Technology

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of the study is to clarify whether patients classified as Latent autoimmune diabetes of the adult (LADA) benefit from early treatment with insulin added to per oral treatment and lifestyle measures.
Detailed Description
Latent autoimmune diabetes of the adult (LADA) is usually defined as a form of diabetes where the onset of diabetes takes place approximately after 30 years of age, where there is presence of beta-cell directed antibodies (mostly anti-GAD) and where there is no clinical need for insulin treatment during the first 6 months after the diagnosis of diabetes. The aetiology and treatment of LADA patients is much less elucidated than is the case for type 1 diabetes (DM1) and type 2 diabetes (DM2). LADA constitutes about 10 % of the total diabetic population in many countries. LADA is therefore more common than insulin-requiring DM1. LADA patients lose beta-cell function faster than patients with DM2. Residual beta-cell function in DM1 is coupled to better metabolic control with lesser degree of hyperglycemia, lesser frequency of hypoglycaemic events and lesser diabetic complications. To retain beta-cell function in LADA patients is thus highly desirable. There are several strategies to retain beta cell function. One therapeutic strategy is to induce some degree of "beta cell rest" by treatment with exogenous insulin. Several observations indicate that such a strategy can have beneficial effects. This is a Scandinavian multicenter non-blinded clinical trial with 78 participants with newly diagnosed LADA. Participants will be randomized to either insulin- or per oral antidiabetic treatment. Participants will be followed up for 2 years after inclusion. Beta cell function and glycemic control will be monitored.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes
Keywords
Latent autoimmune diabetes, adults, Beta cell rest, Insulin secretion

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
64 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Metformin + NPH Insulin
Arm Type
Active Comparator
Arm Description
Patients are treated with metformin during the run-in period (3 months) and also after randomization. By randomization insulin treatment will be added in the form of injections of NPH insulin in the evenings.
Arm Title
Metformin + sitagliptin +/-repaglinid
Arm Type
Active Comparator
Arm Description
Patients are treated with metformin during the run-in period (3 months) and also after randomization. By randomization sitagliptin tablets will be added.If HbA1c after 6 months of treatment is > 10 % above the upper limit of normal,then treatment with repaglinide tablets tree times daily at mealtimes will be added.
Intervention Type
Drug
Intervention Name(s)
metformin+ NPH insulin
Other Intervention Name(s)
Insulatard, Januvia
Intervention Description
Metformin 500 mg + 500 mg + 1000 mg NPH insulin , initially 0.20 U/kg body weight.
Intervention Type
Drug
Intervention Name(s)
metformin + sitagliptin +/- repaglinide
Other Intervention Name(s)
Novonorm
Intervention Description
Metformin 500 mg + 500 mg + 1000 mg Sitagliptin 100 mg x 1 Repaglinide 1 mg x 3
Primary Outcome Measure Information:
Title
insulin secretion
Description
insulin secretion measured by fasting and glucagon-stimulated C-peptide
Time Frame
2 years
Secondary Outcome Measure Information:
Title
glycemic control
Description
glycemic control (HbA1c)
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diabetes diagnosed during 0-3 years before entering the study. Age > or equal to 30 years < or equal to 75 years anti-GAD positivity fasting C-peptide > or equal to 0,3 ng/ml no need for insulin treatment by clinical judgement for at least 3 months following the diagnosis of diabetes. HbA1c > 15 % above the upper limit of normal Exclusion Criteria: Renal insufficiency (plasma creatinine > 150 mol/L) Severe retinopathy (proliferative or pre-proliferative) Severe cardiac disease (NYHA III-IV) Chronic severe illness judged by the investigator Females of reproductive age who wish to become pregnant during the study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Valdemar Grill, med phd
Organizational Affiliation
Department of Cancer Research and Molecular Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Valdemar Grill
City
Trondheim
ZIP/Postal Code
7006
Country
Norway

12. IPD Sharing Statement

Citations:
PubMed Identifier
31148332
Citation
Hals IK, Fiskvik Fleiner H, Reimers N, Astor MC, Filipsson K, Ma Z, Grill V, Bjorklund A. Investigating optimal beta-cell-preserving treatment in latent autoimmune diabetes in adults: Results from a 21-month randomized trial. Diabetes Obes Metab. 2019 Oct;21(10):2219-2227. doi: 10.1111/dom.13797. Epub 2019 Jun 19.
Results Reference
result

Learn more about this trial

Treatment of Latent Autoimmune Diabetes of the Adult

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