Coronary Arteriosclerosis, Hypertension
Conditions
Brief summary
The aim of this trial is to evaluate the efficacy and safety of telmisartan 80 mg administered once daily in patients with documented coronary artery disease (CAD) and a probably cardiovascular risk profile concerning the amelioration of structural alterations and endothelial function. The primary objective of this trial is to evaluate the efficacy in particular with regard to the percentage change of atheroma volume in the femoral artery.The secondary objective is to evaluate the change in the plaque size- assessed by intravascular ultrasound, the increase in Flow Dependent Dilation provoked by intraarterial infusion of three increasing concentrations of Acetylcholine, and the change in seated systolic blood pressure. Endothelial dysfunction is a primary event in atherogenesis and all known cardiovascular risk factors have been associated with endothelial dysfunction before atherosclerotic vascular disease manifests itself clinically. Pivotal to endothelial dysfunction is a disturbance in the function of endothelium-derived nitric oxide (NO). Recently, it could be shown that acute and chronic angiotensin-1 receptor antagonism reversed endothelial dysfunction in atherosclerosis. In experimental atherosclerosis, AT1 receptor blockade appears to have protective effects. Respective potential mechanisms include the prevention of endothelial injury, the augmentation of NO activity, the inhibition of lipid peroxidation and an antiproliferative effect. These findings together with the most recent data that losartan improves endothelial function and NO activity suggest that AT1 receptor antagonism may also be antiatherogenic in patients with atherosclerosis. Angiotensin II influences smooth muscle cell migration, hyperplasia, and hypertrophy. Angiotensin II also enhances production of local superoxide anion, which will inactivate nitric oxide. Inhibition of these reactions by the AT1-Blocker telmisartan may therefore interfere with atherosclerotic plaque formation.
Detailed description
Methodology: 2:1 randomised, double-blind and placebo-controlled parallel-group design Planned/actual number of subjects: Enrolled: 30/33, randomised: 30/22, completed: 30/15 Duration of treatment: 9 months: telmisartan (80 mg) or Placebo (80 mg) Study Hypothesis: The trial is designed as a group comparison of telmisartan 80 mg and placebo, where the treatment groups are randomised in 2:1 relation, to investigate the efficacy of telmisartan on structural alterations and endothelial dysfunction as measured as the percentage change from baseline after 36 weeks of treatment of the atheroma volume in the femoral artery using IVUS . Secondary endpoints are the changes from baseline in the flow dependent dilatation after a acetylcholine challenge which follows a nitro-glycerin bolus, the change of the total atheroma volume, the percentage atheroma volume measured by intravascular ultrasound (IVUS) and the infalmmatory parameters MCP-1, CRP, ox LDL antibodies and sPLA2 activity and amount. In an analysis of covariance using baseline as covariate all endpoints will be investigated. If the assumptions of normal distribution are not fulfilled, nonparametric methods will be applied (Wilcoxon-Mann-Whitney test). Comparison(s): Placebo 80 mg
Interventions
DRUGtelmisartan
DRUGPlacebo
Sponsors
Boehringer Ingelheim
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE
Eligibility
Sex/Gender
ALL
Age
36 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. \> 35 years of age 2. History of coronary artery disease (CAD) 3. Ability to provide written informed consent
Exclusion criteria
1. Pre-menopausal women (last menstruation \< 1 year prior to start of the screening visit) who: 1. are not surgically sterile; and/or 2. are nursing 3. are of child-bearing potential and are NOT practising acceptable means of birth control, do NOT plan to continue using this method throughout the study and do NOT agree to submit to periodic pregnancy testing during participation in studies of \> 3-months duration. Acceptable methods of birth control include oral, implantable or injectable contraceptives 2. Diastolic blood pressure \> 110 mmHg or systolic blood pressure \> 180 mmHg at any visit during the study (run-in or randomised period) 3. Hepatic and/or renal dysfunction as defined by the following laboratory parameters: 1. SGPT(ALT) or SGOT(AST) \> than 2 times the upper limit of normal range 2. Serum creatinine \> 2.3 mg/dL 4. Bilateral renal artery stenosis, renal artery stenosis in a solitary kidney, patients post-renal transplant or with only one kidney 5. Clinically relevant hypokalaemia or hyperkalaemia 6. Uncorrected volume depletion 7. Uncorrected sodium depletion 8. Primary aldosteronism 9. Hereditary fructose intolerance 10. Biliary obstructive disorders 11. Patients who have previously experienced symptoms characteristic of angioedema during treatment with ACE inhibitors or angiotensin II receptor antagonists 12. History of drug or alcohol dependency within 6 months 13. Chronic administration of any medications known to affect blood pressure, except medication allowed by the protocol 14. Any investigational therapy within one month of signing the informed consent form 15. Known hypersensitivity to any component of the formulation 16. Any other clinical condition which, in the opinion of the principal investigator, would not allow safe completion of the protocol and safe administration of telmisartan 17. Stroke within the last 6 months 18. Myocardial infarction within the last 30 days 19. Cardiac surgery within the last 3 months 20. Hyperthyroidosis 21. Hemodynamically relevant valvular disease 22. Restrictive hypertrophic cardiomyopathy 23. Unstable angina pectoris 24. CAD with the indication of bypass surgery.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change of intima/media ratio in the femoral artery measured by intravascular ultrasound (IVUS) | after 39 weeks |
Secondary
| Measure | Time frame |
|---|---|
| Change in plaque size in the femoral artery measured by IVUS | after 39 weeks |
| Increase in FDD (Flow dependent dilation) stimulated by intra-arterial infusion of Acetylcholine (ACH) | after 39 weeks |
| Change in serum inflammatory markers (CRP, MCP-1, oxLDL antibodies, and VCAM) | after 39 weeks |
| Change in seated blood pressure (BP) at trough | after 39 weeks |
Countries
Germany
Outcome results
None listed