Type 2 Diabetes Clinical Trial
Official title:
The Benefit of the Blood Glucose Self Monitoring and a Regular Three-monthly Hemoglobin A1c Profile in Patients With Type 2-diabetes and Conventional Insulin Therapy
The purpose of this randomized, prospective trial is to determine wether (a) a once weekly glucose profile (self monitoring) or (b) a three-monthly report of the actual glycated haemoglobin are effective interventions to improve HbA1c after one year in typ 2-diabetic patients on conventional insulin treatment.
The design is an open, prospective, randomised, multicentre parallel group study. The total
duration will be 5 years with patient recruitment over 4 years and an individual observation
period of 1 year. 300 participants from 43 study centres, hospitals and private practices
were recruited. The study will run for one year and aims to determine, whether there is an
advantage with regard to HbA1c levels when (a) a regular three-monthly HbA1c or (b) a weekly
4-point glucose profile is taken and reported.
After screening, patients will be assigned at random to one of the following study arms:
1. no regular blood-glucose self-monitoring, no regular HbA1c
2. regular blood glucose self monitoring, no regular HbA1c
3. no regular blood glucose self monitoring, regular HbA1c
4. regular blood glucose self monitoring, regular HbA1c
The control for all participants is that urinary glucose should be monitored at least once a
day, preferably in the late morning, as the highest increase in plasma glucose level occurs
after breakfast.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Diagnostic
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