Diabetes Mellitus, Type 2 Clinical Trial
Official title:
AMIT Study - Amaryl M Initiation and Titration Study
Primary Objective:
- To describe the conditions of initiation and titration of Amaryl M, according to
previous treatment:
- initial dose
- titration scheme
- efficacy after 4 months assessed by HbA1C
- tolerability (number and severity of hypoglycaemia)
Secondary Objective:
- Fasting Plasma Glucose
- Weight evolution
n/a
Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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