COMPARISON OF THE EFFICACY OF 3 DOSE LEVELS OF MOEXIPRIL VERSUS PLACEBO AS ADD-ON THERAPY TO HYDROCHLOROTHIAZIDE IN PATIENTS WITH MODERATE HYPERTENSION

This parallel, double-blind trial was designed to evaluate the efficac y of three dose levels of moexipril versus placebo as add-on therapy t o hydrochlorothiazide (HCTZ) in patients with uncomplicated moderate t o severe hypertension. Two hundred patients (aged 25-74 years) with si tting diastolic blood pressure (DBP) between 95 and 114 mm Hg after 4- week treatment with HCTZ 25 mg once daily were randomized to placebo, or moexipril 3.75, 7.5 mg, or 15 mg. BP was measured at 22-26 h postdo se at biweekly visits and at 1, 2, 3, and 4 h postdose after the first dose of double-blind medication. At endpoint, adjusted mean reduction s from baseline sitting DBP were 8.4, 8.8, and 8.9 mm Hg in the moexip ril 3.75-, 7.5-, and 15-mg groups, respectively, as compared with a re duction of 4.6 mm Hg in the placebo group (p = 0.003). The differences in systolic BP (SBP) reductions were statistically significant in fav or of each of the moexipril groups over the placebo group at all troug h time-points. Adjusted mean changes in sitting SBP were 10.9, 12.0, a nd 11.7 mm Hg, respectively, as compared with a reduction of 0.6 mm Hg in the placebo group (p < 0.001). Our results indicate that moexipril and HCTZ constitute a clinically valuable combination in treatment of patients with moderate to severe hypertension.