Diabetes Mellitus, Type 2 Clinical Trial
Official title:
Multi-centre, Open, Randomised, Parallel, Controlled Trial in Type 2 Diabetic Subjects Inadequately Controlled With SU +/ Biguanide Therapy, to Compare the Efficacy and Safety of Repaglinide Combined With Bedtime Insulin vs. Insulin Alone
Verified date | February 2017 |
Source | Novo Nordisk A/S |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This trial is conducted in Europe. The aim of this trial is to compare the efficacy and safety of repaglinide combined with insulin NPH versus biphasic human insulin 30 alone in type 2 diabetics inadequately controlled with sulfonylurea (SU) +/ biguanide therapy
Status | Terminated |
Enrollment | 40 |
Est. completion date | September 20, 2004 |
Est. primary completion date | September 20, 2004 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 40 Years to 75 Years |
Eligibility |
Inclusion Criteria: - HbA1c: 7.5-11.0% on current therapy - OHA (oral hypoglycaemic agent) treatment for a minimum of two years - BMI (body mass index): 25-32 kg/m2 |
Country | Name | City | State |
---|---|---|---|
Greece | Novo Nordisk Investigational Site | Athens |
Lead Sponsor | Collaborator |
---|---|
Novo Nordisk A/S |
Greece,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | HbA1c | after 20 weeks of treatment | ||
Secondary | Fasting blood glucose (FBG) | |||
Secondary | Incidence of hypoglycaemic episodes | |||
Secondary | Adverse events |
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