Impaired glucose tolerance Nutritional, Metabolic, Endocrine Diabetes
Conditions
Interventions
Subjects valid for inclusion were randomly assigned to acarbose 50 mg tds, metformin 500 mg tds, a combination of the two, or matching placebo.
Sponsors
Bayer plc and Merck-Lipha (UK)
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Subjects aged 30 to 70 years inclusive, with fasting hyperglycaemia; defined as a fasting plasma glucose (FPG) level =5.5 mmol/l and <7.8 mmol/l on two occasions at least 1 week apart
Exclusion criteria
Exclusion criteria: Not provided at time of registration
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Not provided at time of registration | — |
Secondary
| Measure | Time frame |
|---|---|
| Not provided at time of registration | — |
Countries
United Kingdom
Outcome results
None listed