Why the study?
Does the combination of ramipril and felodipine ER improve blood pressure reduction and tolerability compared to monotherapy or placebo in patients with mild-to-moderate hypertension?
Does the combination of ramipril and felodipine ER improve blood pressure reduction and tolerability compared to monotherapy or placebo in patients with mild-to-moderate hypertension?
The combination of ramipril 5 mg and felodipine ER 5 mg offers an optimal balance of antihypertensive efficacy and tolerability for patients with mild-to-moderate hypertension.
Supports ramipril-felodipine ER 5/5 mg for initial hypertension therapy; extends RCT evidence favoring low-dose ACEI-CCB combinations over CCB monotherapy.
The aim of the study was to identify the most appropriate dosage combination of ramipril and felodipine ER (an extended release tablet) for mild-to-moderate hypertension. Hypertensive patients (N = 507) with supinediastolic blood pressure (DBP) values between 100-115 mm Hg were included in a randomized, multicenter, double-blind study of 3x4 factorial design with a 2-4 week single-blind, placebo run-in and 6 week active treatment phase. The patients were randomized to 12 groups: placebo, ramipril (2.5, 5, 10 mg), felodipine ER (5, 10 mg), or ramipril-felodipine ER combinations (2.5/5 mg, 2.5/10 mg, 5/5 mg, 5/10 mg, 10/5 mg, 10/10 mg). Although the greatest reductions in blood pressure were observed with ramipril-felodipine ER (10/10 mg), consideration of the antihypertensive efficacy and safety factors suggest that the ramipril-felodipine ER (5/5 mg) combination has the best efficacy/tolerability ratio of the combinations tested. The incidence of adverse events with ramipril-felodipine ER combination therapy was similar to that with felodipine ER monotherapy, but peripheral edema, tachycardia and vasodilatation occurred less frequently with ramipril-felodipine ER (5/5 mg) combination than with felodipine ER monotherapy. The combination of ramipril-felodipine ER (5/5 mg) can be considered to be the most suitable option for hypertensive patients with an inadequate response to either of the monocomponents.
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Scholze et al. (1999) studied this question.
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