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Effect of Metformin in Patients With Type-1 Diabetes With Inadequate Glycaemic Control by Insulin and Diet

Primary Purpose

Diabetes Mellitus, Type 1

Status
Completed
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Metformin
Placebo.
Placebo.
Sponsored by
Steno Diabetes Center Copenhagen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes Mellitus, Type 1

Eligibility Criteria

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

Inclusion Criteria: HbA1c > 8.5% for more than one year prior to enrolment. Diabetes-duration > 5 years. Age at onset of diabetes < 35 years Fasting C-peptide < 300 pmol/l Age > 18 years at enrolment. Exclusion Criteria: Clinical or biochemical signs of kidney-, liver- or heart-failure. Other coexisting serious morbidity, which will affect the study-participation or outcome of the study i.e. cancer. Known abuse of any medication or alcohol Hypoglycaemia unawareness. Pregnancy or planned pregnancy in the study-period.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm Type

    Placebo Comparator

    Active Comparator

    Placebo Comparator

    Arm Label

    1

    2

    3

    Arm Description

    Single-blind placebo run-in period. Duration one month.

    Metformin 2000 mg, double-masked randomized during 12 months.

    Placebo, double-masked randomized during 12 months.

    Outcomes

    Primary Outcome Measures

    HbA1c - difference between final visit and baseline.

    Secondary Outcome Measures

    Absolute HbA1c
    Number of mild and severe hypoglycaemia with or without measurements of blood-glucose.
    Insulin-dose
    The following parameters are measured at baseline and at the final visit after 12 months of intervention:
    Plasma-PAI-antigen and -activity, t-PA-antigen- and activity.
    Plasma-fibrinogen
    Serum-albumin
    Markers of endothelial dysfunction: Von Willebrand Factor, ICAM, VCAM, Amadori-protein, selectin and endothelin.
    Plasma-homocysteine
    Asymmetric DiMethylArginine - ADMA
    Urine-albumin-excretion in three 24 hour urine-collections
    Blood-pressure in the sitting position after 10 minutes of rest.
    Fasting lipid-profile (total-cholesterol, LDL-cholesterol, HDL-cholesterol, VLDL-cholesterol and triglycerides), small-dense-LDL, Lp(a) and Apo-B100.
    Weight, BMI and Waist-hip-ratio
    White blood-cell-count, hs-CRP, Interleukin-6 and TNF-alfa.
    Serum-creatinine, sodium, potassium, ASAT, alkaline phosphatase, Factor 2, 7, 10, Cobalamin, Erythrocyte-folate and Haemoglobin-concentration.
    Extra blood- and urine-samples will be stored at -80 degrees Celsius for potential extra analyses after closure of the study. DNA will be stored for later pharmaco-genetic analysis.

    Full Information

    First Posted
    July 1, 2005
    Last Updated
    December 5, 2008
    Sponsor
    Steno Diabetes Center Copenhagen
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00118937
    Brief Title
    Effect of Metformin in Patients With Type-1 Diabetes With Inadequate Glycaemic Control by Insulin and Diet
    Official Title
    Effect of Metformin On Glycaemic Control and Non-Glycaemic Cardiovascular Risk-Factors in Patients With Type-1 Diabetes, With Long-Standing Inadequate Glycaemic Control by Insulin and Diet
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    December 2008
    Overall Recruitment Status
    Completed
    Study Start Date
    December 2003 (undefined)
    Primary Completion Date
    August 2006 (Actual)
    Study Completion Date
    August 2006 (Actual)

    3. Sponsor/Collaborators

    Name of the Sponsor
    Steno Diabetes Center Copenhagen

    4. Oversight

    5. Study Description

    Brief Summary
    Ninety percent of patients with type-1-diabetes will develop late-diabetic complications in the eyes, kidneys, nervous- or cardiovascular-system. Poor glycaemic control is an important risk-factor for development of these late-diabetic complications. The Diabetes Control and Complications Trial (DCCT)-study showed, that improved glycaemic control can prevent the development and progression of these late-diabetic complications. Until now treatment with insulin- and diet-therapy has been the only treatment-modalities available to improve the glycaemic control in patients with type-1-diabetes. A substantial number of these patients still have long-standing poor glycaemic control despite intensive treatment with insulin- and diet-therapy. The antidiabetic drug metformin has shown to be able to improve the glycaemic control in combination with insulin and furthermore reduce both mortality and the risk of developing cardiovascular disease in patients with type-2-diabetes. Only few small studies have investigated the effect of treatment with metformin in patients with type-1-diabetes. These studies have suggested a positive effect of metformin in these patients too. Method: 100 patients with type-1-diabetes with persistent poor glycaemic control i.e. HbA1c > 8.5% during the last 12 months are eligible. Patients are treated for one month with placebo. Hereafter half of the patients will be treated with metformin and the other half continues with placebo for 12 months both as add-on therapy. All patients are continuing ongoing treatment with insulin throughout the study. Before and after the start of treatment with metformin the effect on glycaemic control and other known risk-factors for development of cardiovascular disease i. e. blood-pressure, fasting lipids, urine-albumine-excretion, endothelial dysfunction, inflammation, fibrinolysis etc. is assessed. This study will show if treatment with metformin can improve the glycaemic control and hereby the prognosis of patients with type-1-diabetes with persistent poor glycaemic control despite intensive treatment with insulin- and diet-therapy. This group of patients suffers the highest risk of developing late-diabetic complications with reduced quality of life and life-expectancy as a consequence.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Diabetes Mellitus, Type 1

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 4
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantCare ProviderInvestigatorOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    100 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    1
    Arm Type
    Placebo Comparator
    Arm Description
    Single-blind placebo run-in period. Duration one month.
    Arm Title
    2
    Arm Type
    Active Comparator
    Arm Description
    Metformin 2000 mg, double-masked randomized during 12 months.
    Arm Title
    3
    Arm Type
    Placebo Comparator
    Arm Description
    Placebo, double-masked randomized during 12 months.
    Intervention Type
    Drug
    Intervention Name(s)
    Metformin
    Intervention Description
    Tablet Metformin 500 mg, Dosage: 1000 mg two times daily (2000 mg total daily dose).
    Intervention Type
    Drug
    Intervention Name(s)
    Placebo.
    Intervention Description
    Tablet Placebo (corresponding to 500 mg metformin). Dosage: 1 tablet per day.
    Intervention Type
    Drug
    Intervention Name(s)
    Placebo.
    Intervention Description
    Tablet Placebo (corresponding to 500 mg metformin). Dosage: 2 tablets two times daily.
    Primary Outcome Measure Information:
    Title
    HbA1c - difference between final visit and baseline.
    Secondary Outcome Measure Information:
    Title
    Absolute HbA1c
    Title
    Number of mild and severe hypoglycaemia with or without measurements of blood-glucose.
    Title
    Insulin-dose
    Title
    The following parameters are measured at baseline and at the final visit after 12 months of intervention:
    Title
    Plasma-PAI-antigen and -activity, t-PA-antigen- and activity.
    Title
    Plasma-fibrinogen
    Title
    Serum-albumin
    Title
    Markers of endothelial dysfunction: Von Willebrand Factor, ICAM, VCAM, Amadori-protein, selectin and endothelin.
    Title
    Plasma-homocysteine
    Title
    Asymmetric DiMethylArginine - ADMA
    Title
    Urine-albumin-excretion in three 24 hour urine-collections
    Title
    Blood-pressure in the sitting position after 10 minutes of rest.
    Title
    Fasting lipid-profile (total-cholesterol, LDL-cholesterol, HDL-cholesterol, VLDL-cholesterol and triglycerides), small-dense-LDL, Lp(a) and Apo-B100.
    Title
    Weight, BMI and Waist-hip-ratio
    Title
    White blood-cell-count, hs-CRP, Interleukin-6 and TNF-alfa.
    Title
    Serum-creatinine, sodium, potassium, ASAT, alkaline phosphatase, Factor 2, 7, 10, Cobalamin, Erythrocyte-folate and Haemoglobin-concentration.
    Title
    Extra blood- and urine-samples will be stored at -80 degrees Celsius for potential extra analyses after closure of the study. DNA will be stored for later pharmaco-genetic analysis.

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: HbA1c > 8.5% for more than one year prior to enrolment. Diabetes-duration > 5 years. Age at onset of diabetes < 35 years Fasting C-peptide < 300 pmol/l Age > 18 years at enrolment. Exclusion Criteria: Clinical or biochemical signs of kidney-, liver- or heart-failure. Other coexisting serious morbidity, which will affect the study-participation or outcome of the study i.e. cancer. Known abuse of any medication or alcohol Hypoglycaemia unawareness. Pregnancy or planned pregnancy in the study-period.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Allan A Vaag, M.D., chief physician
    Organizational Affiliation
    Steno Diabetes Center Copenhagen
    Official's Role
    Study Chair
    First Name & Middle Initial & Last Name & Degree
    Soeren S Lund, M. D.
    Organizational Affiliation
    Steno Diabetes Center Copenhagen
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    18852875
    Citation
    Lund SS, Tarnow L, Astrup AS, Hovind P, Jacobsen PK, Alibegovic AC, Parving I, Pietraszek L, Frandsen M, Rossing P, Parving HH, Vaag AA. Effect of adjunct metformin treatment in patients with type-1 diabetes and persistent inadequate glycaemic control. A randomized study. PLoS One. 2008;3(10):e3363. doi: 10.1371/journal.pone.0003363. Epub 2008 Oct 9.
    Results Reference
    derived

    Learn more about this trial

    Effect of Metformin in Patients With Type-1 Diabetes With Inadequate Glycaemic Control by Insulin and Diet

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