Improving insulin treatment
Not Applicable
Completed
- Conditions
- utritional, Metabolic, Endocrine: DiabetesNutritional, Metabolic, EndocrineInsulin-dependent diabetes mellitus
- Registration Number
- ISRCTN79558333
- Lead Sponsor
- Department of Health
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
1. Type 1 diabetes
2. >2 years duration
3. Clinical decision for glargine/novorapid therapy independently of the study
4. Fully informed and consented
Exclusion Criteria
Does not match inclusion criteria
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To see if adjusting pre-prandial insulin on the basis of post-prandial measurements is feasible as a clinical approach in the routine clinical situation and to explore the possibility that it might improve overall diabetes control.
- Secondary Outcome Measures
Name Time Method ot provided at time of registration