Diabetes Mellitus Clinical Trial
— GlyCEDIAOfficial title:
Glycemic Control Assessed by Continuous Glucose Monitoring in Hemodialyzed Patients With Diabetes Mellitus Treated Via the Basal-Bolus Detemir-Aspart Insulin Regimen: A Pilot Study
The purpose of the study is to evaluate the effect of the basal-bolus detemir-aspart insulin regimen coupled with continuous glucose monitoring (CGM) on glycemic control in hemodialyzed patients with diabetes
| Status | Completed |
| Enrollment | 38 |
| Est. completion date | September 2012 |
| Est. primary completion date | September 2012 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 18 Years to 83 Years |
| Eligibility |
Inclusion Criteria: - age between 18 and 83 years - diagnosis of type 1 or type 2 diabetes - treatment with insulin injections or oral hypoglycemic agents - HbA1c = 7% (i.e., 53 mmol/mol) - on hemodialysis for more than three months Exclusion Criteria: - unstable anemia or blood transfusions within the two months prior to the beginning of the study - a life expectancy of less than 1 year - chronic inflammatory disease - evolutive cancer requiring steroid treatment, chemotherapy, radiotherapy, or programmed surgery - noncompliant patients |
Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| France | Regional Hospital of Colmar | Colmar | |
| France | Regional Hospital of Mulhouse | Mulhouse | |
| France | Sainte Anne Hospital | Strasbourg | |
| France | University Hospital of Strasbourg | Strasbourg | |
| France | Regional Hospital of Valenciennes | Valenciennes |
| Lead Sponsor | Collaborator |
|---|---|
| Centre Europeen d'Etude du Diabete | Abbott, Novo Nordisk A/S |
France,
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* Note: There are 30 references in all — Click here to view all references
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Mean plasma glucose level measured 3 times just before the first hemodialysis session | Determination by the glucose dehydrogenase method | Baseline and at 3 months of treatment | No |
| Secondary | HbA1c | Measured by high-performance liquid chromatography | Baseline and at 3 months of treatment | No |
| Secondary | Body weight | Baseline and at 1 month and 3 months of treatment | No | |
| Secondary | Insulin requirements | IU per day | Baseline and at 1 month and 3 months of treatment | No |
| Secondary | Symptomatic hypoglycemia | Number of glycemia < 60 mg/dl per patient and per month | Baseline and at 1 month and 3 months of treatment | No |
| Secondary | Continuous glucose monitoring parameters | Including: mean continuous glucose monitoring glucose values, within-subjects standard deviation (wSD) and coefficient of variation (wCV = wSD/mean), mean amplitude of glycemic excursion (MAGE), frequency of glucose values under 60 mg/dl, and frequency of glucose values higher than 180 mg/dl | Baseline and at 1 month and 3 months of treatment | No |
| Secondary | Deaths and major cardiovascular events | All-cause mortality Major cardiovascular events including: myocardial infarction, stroke, and peripheral vascular disease | Baseline and at 3 months of treatment | Yes |
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