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Journal of cardiovascular pharmacology

Publication date: 1985-01-01
Pages: S128 - S129
Publisher: Lippincott, Williams & Wilkins

Author:

Fagard, Robert
Fiocchi, R ; Lijnen, Paul ; Staessen, Jan A ; Amery, A

Keywords:

Adult, Cardiac Output, Clinical Trials, Double-Blind Method, Exertion, Female, Heart Rate, Hemodynamic Processes, Humans, Hypertension, Ketanserin, Male, Methoxamine, Phenylephrine, Piperidines, Random Allocation, Serotonin Antagonists, Stroke Volume, Vascular Resistance, Science & Technology, Life Sciences & Biomedicine, Cardiac & Cardiovascular Systems, Pharmacology & Pharmacy, Cardiovascular System & Cardiology, Clinical Trials as Topic, Hemodynamics, Physical Exertion, 1102 Cardiorespiratory Medicine and Haematology, 1115 Pharmacology and Pharmaceutical Sciences, Cardiovascular System & Hematology, 3201 Cardiovascular medicine and haematology, 3214 Pharmacology and pharmaceutical sciences

Abstract:

Ketanserin (120 mg/day) or placebo was given orally to 14 patients with mild to moderate essential hypertension according to a double-blind crossover protocol, each treatment period lasting 6 weeks. Resting intraarterial pressure in the recumbent position was reduced from 150/84 to 141/77 mm Hg; the hypotensive effect persisted throughout an uninterrupted graded exercise test to the point of exhaustion. The hemodynamic effects were similar at rest and during exercise. Overall, systemic vascular resistance decreased by 14%, heart rate fell by 5%, but stroke volume and cardiac output increased. The pressor responses to methoxamine and to phenylephrine were reduced by ketanserin.