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Clinical Trials/NCT00121966
NCT00121966
Completed
Phase 4

South Danish Diabetes Study: A Prospective Randomised Multi-Centre Study for the Evaluation of the Optimal Pharmacological Antidiabetic Treatment of Type 2 Diabetes Mellitus

Odense University Hospital1 site in 1 country400 target enrollmentJanuary 2003

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Type 2 Diabetes Mellitus
Sponsor
Odense University Hospital
Enrollment
400
Locations
1
Primary Endpoint
HbA1c following two years of treatment
Status
Completed
Last Updated
17 years ago

Overview

Brief Summary

The primary objective of this study is:

  • To investigate whether insulin aspart with meals is better than a standard treatment with insulin NPH at bedtime, evaluated by HbA1c.

The secondary objectives of this study are:

  • To study if a combination treatment with metformin and/or rosiglitazone and insulin aspart with meals is better than a standard treatment with insulin NPH combined with one or more of the above oral antidiabetic drugs. According to the hypothesis, special focus will be given to the treatment group with insulin aspart combined with metformin and rosiglitazone. The treatment effect will be evaluated by HbA1c.

  • To examine the effects of the treatments on glucose metabolism and beta cell function, evaluated by diurnal blood glucose, fasting plasma glucose, insulin, C-peptide, and lactate.

  • To examine the effects of the treatments on cardiovascular risk factors evaluated by serum lipid profiles, serum free fatty acids, urine albumin/creatinine ratio, and electrocardiogram (ECG).

  • To quantify and describe the patients' subjective experiences of the two different insulin treatments (quality of life assessment)

  • To examine patients with type 2 diabetes for the presence of variability in a series of genes, which are known to or are assumed to:

    • affect the long term outcome;
    • determine the responsiveness to treatment with diet, exercise and drugs targeting the known risk markers for late diabetic complications; and
    • after intervention, to analyse the complex interrelationships between genotypes and clinical endpoints and the responsiveness to actual treatment modalities.
Registry
clinicaltrials.gov
Start Date
January 2003
End Date
July 2007
Last Updated
17 years ago
Study Type
Interventional
Study Design
Factorial
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Ages between 30 and 70 years
  • Fasting C-peptide \>300 pmol/l
  • Body mass index (BMI) \> 25 kg/m2
  • Diabetes for more than 2 years
  • Pharmacological antidiabetic treatment for more than 3 months
  • 7.0%\<HbA1c\<12.0% at randomisation
  • Patient willing to sign informed consent
  • Fertile women: negative pregnancy test and use of oral or intra-uterine contraception or depot gestagen.

Exclusion Criteria

  • S-creatinine \> 120 μmol/l
  • History of intolerance to metformin or glitazones
  • S-ALAT/S-ASAT \> 2.5 x upper normal limit
  • Total cholesterol \> 10 mmol/l
  • Total triglyceride \> 8 mmol/l
  • Hemoglobin (Hb) \< normal range
  • Treatment with glitazone preceding 30 days New York Heart Association (NYHA) functional class III or IV
  • Night work
  • Present or planned pregnancy
  • Poor vision impeding insulin administration

Outcomes

Primary Outcomes

HbA1c following two years of treatment

Secondary Outcomes

  • fasting blood glucose
  • body weight
  • blood pressure
  • free fatty acids
  • lactate
  • urine glucose
  • diurnal blood glucose profiles (self monitored and continuously monitored)
  • fasting insulin, proinsulin-C-peptide
  • fasting cholesterol (including HDL, LDL, and triglyceride)
  • urine albumin/creatinine ratio

Study Sites (1)

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