Fifteen out-patients with moderate hypertension were randomly and sequentially treated with atenolol, indapamide and a combination of the two drugs after a wash-out period of at least 1 week and a 2-week placebo run-in period. The duration of treatment was 4 weeks in each case. The dosage was 2.5 mg indapamide and 100 mg atenolol, in single tablets which were taken at 11.00 hours. All the treatment regimens produced a highly significant (p < 0.001) reduction in systolic and diastolic, supine and standing blood pressure; these reductions were not significantly different for the single drugs but were significantly greater for the combined therapy. The number of patients reaching the end-point of a diastolic blood pressure of 95 mmHg or less was the same with either atenolol or indapamide, i.e. 7 (46.6%), but was greater with the combined therapy, i.e. 10 (66.6%). A significant (p < 0.001) reduction in pulse rate was observed with the treatments involving atenolol. Acceptability of the treatments was very good; the number of volunteered and elicited complaints during the different treatments being less compared to the placebo period, particularly for the combined treatment. No significant difference was observed in the blood biochemistry tests. The results are discussed in light of the mechanisms of action of the two drugs, which seem well integrated with each other, and the duration of the antihypertensive effect, which allows a single administration with consequent good treatment compliance.

Indapamide and atenolol in the treatment of hypertension: Double-blind comparative and combination study / O., De Divitiis; DI SOMMA, Salvatore; M., Petitto; S., Fazio; V., Ligouri. - In: CURRENT MEDICAL RESEARCH AND OPINION. - ISSN 0300-7995. - STAMPA. - 8:7(1983), pp. 493-500. [10.1185/03007998309109788]

Indapamide and atenolol in the treatment of hypertension: Double-blind comparative and combination study

DI SOMMA, Salvatore;
1983

Abstract

Fifteen out-patients with moderate hypertension were randomly and sequentially treated with atenolol, indapamide and a combination of the two drugs after a wash-out period of at least 1 week and a 2-week placebo run-in period. The duration of treatment was 4 weeks in each case. The dosage was 2.5 mg indapamide and 100 mg atenolol, in single tablets which were taken at 11.00 hours. All the treatment regimens produced a highly significant (p < 0.001) reduction in systolic and diastolic, supine and standing blood pressure; these reductions were not significantly different for the single drugs but were significantly greater for the combined therapy. The number of patients reaching the end-point of a diastolic blood pressure of 95 mmHg or less was the same with either atenolol or indapamide, i.e. 7 (46.6%), but was greater with the combined therapy, i.e. 10 (66.6%). A significant (p < 0.001) reduction in pulse rate was observed with the treatments involving atenolol. Acceptability of the treatments was very good; the number of volunteered and elicited complaints during the different treatments being less compared to the placebo period, particularly for the combined treatment. No significant difference was observed in the blood biochemistry tests. The results are discussed in light of the mechanisms of action of the two drugs, which seem well integrated with each other, and the duration of the antihypertensive effect, which allows a single administration with consequent good treatment compliance.
1983
adult; atenolol; clinical trials as topic; combination; diuretics; double-blind method; drug therapy; female; humans; hypertension; indapamide; male; middle aged; random allocation; therapeutic use
01 Pubblicazione su rivista::01a Articolo in rivista
Indapamide and atenolol in the treatment of hypertension: Double-blind comparative and combination study / O., De Divitiis; DI SOMMA, Salvatore; M., Petitto; S., Fazio; V., Ligouri. - In: CURRENT MEDICAL RESEARCH AND OPINION. - ISSN 0300-7995. - STAMPA. - 8:7(1983), pp. 493-500. [10.1185/03007998309109788]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/445263
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