| Literature DB >> 2556172 |
H J Gomez1, V J Cirillo, J A Sromovsky, E S Otterbein, W C Shaw, J E Rush, S G Chrysant, A H Gradman, A S Leon, E P MacCarthy.
Abstract
1. This was a multicentre, double-blind, parallel study in 216 patients with mild to moderate (supine diastolic blood pressure = 95-115 mm Hg) essential hypertension. 2. After a 4-week placebo washout, patients were randomized to placebo or lisinopril 1.25, 5.20 or 80 mg once daily for 6 consecutive weeks. Supine and erect blood pressure was measured 24 h postdose at the end of weeks -2, 0, 2, 4, and 6. 3. There was a linear dose-response relationship for both supine and erect blood pressure. Diastolic blood pressure reductions in the lisinopril 20 and 80 mg day-1 groups were significantly greater than in the placebo or lisinopril 1.25 and 5 mg day-1 groups. 4. Lisinopril, at doses up to 80 mg day-1, was well tolerated.Entities:
Mesh:
Substances:
Year: 1989 PMID: 2556172 PMCID: PMC1379991 DOI: 10.1111/j.1365-2125.1989.tb03521.x
Source DB: PubMed Journal: Br J Clin Pharmacol ISSN: 0306-5251 Impact factor: 4.335