Angina Pectoris, Diabetes Mellitus, Type 2
Conditions
Keywords
Angina, Ischaemic heart disease, Diabetes
Brief summary
The principle objective of the trial is to compare rosiglitazone to gliclazide in patients with type 2 diabetes mellitus and chronic stable angina to see how the subjects' angina status changes. Angina status will be measured via exercise tolerance testing, 24-hour ECG testing and angina quality of life questionnaire.
Detailed description
Ischaemic heart disease is one of the main complications of type 2 diabetes mellitus, both in terms of morbidity and mortality. Reducing plasma glucose with hypoglycaemic agents has not been shown to improve cardiovascular mortality or morbidity. Chronic stable angina is a common problem in patients with type 2 diabetes mellitus. We postulate that in subjects with uncontrolled type 2 diabetes mellitus (Hba1c \>7.5%), on metformin therapy, and chronic stable angina that the addition of the insulin sensitiser, rosiglitazone to control their diabetes will improve their angina when compared to the addition of the hypoglycaemic agent gliclazide. This hypothesis is based on the fact that insulin resistance is an upstream mechanism common to both conditions. We will randomise such patients to 3 months therapy of rosiglitazone or gliclazide for 3 months, comparing angina status before and after by way of full Bruce protocol exercise testing, 24 hour ST segment analysis and angina questionnaire.
Interventions
DRUGRosiglitazone
DRUGGliclazide (Comparison drug)
Sponsors
GlaxoSmithKline
University of Glasgow
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Chronic stable angina with ongoing symptoms. (The treatment goal being an improvement in symptoms) * Participants will have uncontrolled diabetes (Hba1c\>7.5) on metformin monotherapy (so the diabetes is not over treated) * Participants will be diabetic for less than 8 years.
Exclusion criteria
* Renal impairment (creatinine \>130mmol/l) * Hepatic Impairment (ALT\>70U/l, AST\>80U/l) * Any clinical signs of heart failure * Physical disability precluding treadmill exercise tolerance testing * Abnormal resting ECG (left or right bundle-branch block, left or right ventricular hypertrophy, ventricular preexcitation, Q-wave myocardial infarction, digitalis therapy) * Women of childbearing potential * Women who are breastfeeding
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Angina status at 3 months | — |
Secondary
| Measure | Time frame |
|---|---|
| Pulse wave velocity at 3 months | — |
| Small vessel function at 3 months | — |
| Haemostatic markers at 3 months | — |
| Biochemical markers of inflammation at 3 months | — |
Countries
United Kingdom
Outcome results
None listed