Abstract | BACKGROUND: METHODS: After a 2- to 4-week placebo washout period, both drugs were administered once daily and taken for 12 weeks. Blood pressure was measured 24 hours after treatment administration. RESULTS: Systolic and diastolic blood pressure changes from baseline to week 12 were similar for both the bisoprolol and amlodipine groups (-20. 0/-4.5 mm Hg and -19.6/-2.4 mm Hg, respectively). Overall adverse events for bisoprolol and amlodipine were 39% and 40%, respectively. Changes in quality of life scores were +2.5 for bisoprolol and +3.2 for amlodipine, with a positive change indicating improvement. CONCLUSIONS:
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Authors | A Benetos, S Consoli, A Safavian, A Dubanchet, M Safar |
Journal | American heart journal
(Am Heart J)
Vol. 140
Issue 4
Pg. E11
(Oct 2000)
ISSN: 1097-6744 [Electronic] United States |
PMID | 11011336
(Publication Type: Clinical Trial, Comment, Comparative Study, Journal Article, Multicenter Study, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Chemical References |
- Adrenergic beta-Antagonists
- Calcium Channel Blockers
- Diuretics
- Sodium Chloride Symporter Inhibitors
- Hydrochlorothiazide
- Amlodipine
- Bisoprolol
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Topics |
- Adrenergic beta-Antagonists
(therapeutic use)
- Aged
- Amlodipine
(therapeutic use)
- Bisoprolol
(therapeutic use)
- Blood Pressure
(drug effects, physiology)
- Blood Pressure Monitoring, Ambulatory
- Calcium Channel Blockers
(therapeutic use)
- Circadian Rhythm
(physiology)
- Diuretics
- Double-Blind Method
- Drug Therapy, Combination
- Female
- Humans
- Hydrochlorothiazide
(therapeutic use)
- Hypertension
(drug therapy, physiopathology, psychology)
- Male
- Middle Aged
- Quality of Life
- Safety
- Sodium Chloride Symporter Inhibitors
(therapeutic use)
- Systole
- Treatment Outcome
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