Table 2.
Trial name | Patients randomized (n) | Characteristics of study population | Drugs | Duration (years) | Primary endpoint |
---|---|---|---|---|---|
Heart Outcomes Prevention Evaluation (HOPE)11 |
9541 | Age ≥55 years with one high-risk condition | Ramipril Placebo |
4.5 | Ramipril 14.0% versus placebo 17.8% (P < 0.001) |
Losartan Intervention For Endpoint reduction in hypertension (LIFE)12 | 9193 | Hypertension and left ventricular hypertrophy | Losartan Atenolol |
4.8 | Losartan 11.0% versus atenolol 12.8% (P = 0.021) |
Anglo-Scandinavian Cardiac Outcome Trial (ASCOT) blood pressure-lowering arm13 | 19,257 | Hypertension with ≥3 specified risk factors | Amlodipine ± perindopril Atenolol ± bendroflumethiazide-K |
5.0 | Amlodipine-based 4.5% versus atenolol-based 4.9% (P = 0.105) |
Action in Diabetes and Vascular Disease: Preterax and Diamicron-Controlled Evaluation Trial (ADVANCE)14 | 11,140 | Diabetes mellitus | Perindopril ± indapamide Placebo |
4.3 | Perindopril + indapamide 15.5% versus placebo 16.8% (P = 0.04) |
Ongoing Telmisartan alone and in Combination with Ramipril Global Endpoint Trial (ONTARGET)15 | 25,620 | High-risk patients with coronary, peripheral arterial, or cerebrovascular disease, or diabetic patients with target organ damage | Ramipril Telmisartan Ramipril + telmisartan |
4.7 | Ramipril 16.5% versus telmisartan 16.7% versus ramipril + telmisartan 16.3% |
Study in ACE Intolerant Subjects with Cardiovascular Disease (TRANSCEND)16 | 6666 | As ONTARGET study with angiotensin-converting enzyme inhibitor intolerance | Telmisartan Placebo |
4.7 | Telmisartan 15.7% versus placebo 17.0% (P = 0.22) |
Avoiding Cardiovascular Events through Combination Therapy in Patients Living with Systolic Hypertension (ACCOMPLISH)17 | 11,506 | High-risk hypertensive patients | Benazepril + amlodipine Benazepril + hydrochlorothiazide |
3.0 | Benazepril + amlodipine 9.6% versus benazepril + hydrochlorothiazide 11.6% (P < 0.001) |