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

This study has been completed.
Sponsor:
Information provided by:
Steno Diabetes Center
ClinicalTrials.gov Identifier:
NCT00118937
First received: July 1, 2005
Last updated: December 5, 2008
Last verified: December 2008
  Purpose

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.


Condition Intervention Phase
Diabetes Mellitus, Type 1
Drug: Metformin
Drug: Placebo.
Phase 4

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
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

Resource links provided by NLM:


Further study details as provided by Steno Diabetes Center:

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.

Enrollment: 100
Study Start Date: December 2003
Study Completion Date: August 2006
Primary Completion Date: August 2006 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Placebo Comparator: 1
Single-blind placebo run-in period. Duration one month.
Drug: Placebo.
Tablet Placebo (corresponding to 500 mg metformin). Dosage: 1 tablet per day.
Active Comparator: 2
Metformin 2000 mg, double-masked randomized during 12 months.
Drug: Metformin
Tablet Metformin 500 mg, Dosage: 1000 mg two times daily (2000 mg total daily dose).
Placebo Comparator: 3
Placebo, double-masked randomized during 12 months.
Drug: Placebo.
Tablet Placebo (corresponding to 500 mg metformin). Dosage: 2 tablets two times daily.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
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.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00118937

Sponsors and Collaborators
Steno Diabetes Center
Investigators
Study Chair: Allan A Vaag, M.D., chief physician Steno Diabetes Center
Principal Investigator: Soeren S Lund, M. D. Steno Diabetes Center
  More Information

No publications provided by Steno Diabetes Center

Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
ClinicalTrials.gov Identifier: NCT00118937     History of Changes
Other Study ID Numbers: Type-1-Metformin
Study First Received: July 1, 2005
Last Updated: December 5, 2008
Health Authority: Denmark: Danish Medicines Agency

Additional relevant MeSH terms:
Diabetes Mellitus
Diabetes Mellitus, Type 1
Glucose Metabolism Disorders
Metabolic Diseases
Endocrine System Diseases
Autoimmune Diseases
Immune System Diseases
Metformin
Hypoglycemic Agents
Physiological Effects of Drugs
Pharmacologic Actions

ClinicalTrials.gov processed this record on July 22, 2014