Abstract | BACKGROUND: METHODS: One hundred and eighty-one patients with mild-to-moderate primary hypertension were assigned in this randomized, single-blind, parallel-group study and were randomly divided into group A ( benazepril 10 mg/ lercanidipine 10 mg) and group B ( benazepril 10 mg) for 8 weeks. At 4 weeks, the dosage of Benazepril was titrated up to 20 mg if the diastolic blood pressure (DBP) remained ≥ 90 mmHg. BP control and side effects were evaluated at the end of 1, 4 and 8 weeks. RESULTS: The baseline characteristics of the two groups were similar. The BP in both groups decreased from the baseline (P < 0.05). At the end of 4 and 8 weeks, Benazepril/ Lercanidipine produced greater BP reduction than Benazepril alone (P < 0.05). The comparison of the rate of BP control for the benazepril/ lercanidipine and benazepril groups at the end of 1, 4, and 8 weeks were 41.2% vs. 37.6% (P > 0.05), 67.1% vs. 44.7% (P < 0.05), and 71.8% vs. 45.9% (P < 0.05). There was no significant difference of side effects between the two groups. CONCLUSION:
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Authors | Ting Chen, Guang-Hui Chen, Ting-Shu Yang, Zhen-Yu Zhong, Wei-Shuai An, Xiao-Xia Zhang, Jia-Dan Li |
Journal | Chinese medical journal
(Chin Med J (Engl))
Vol. 126
Issue 12
Pg. 2286-90
(Jun 2013)
ISSN: 2542-5641 [Electronic] China |
PMID | 23786940
(Publication Type: Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Chemical References |
- Angiotensin-Converting Enzyme Inhibitors
- Benzazepines
- Calcium Channel Blockers
- Dihydropyridines
- benazepril
- lercanidipine
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Topics |
- Aged
- Angiotensin-Converting Enzyme Inhibitors
(therapeutic use)
- Benzazepines
(administration & dosage, adverse effects, therapeutic use)
- Blood Pressure
(drug effects)
- Calcium Channel Blockers
(administration & dosage)
- Dihydropyridines
(administration & dosage, adverse effects)
- Drug Therapy, Combination
- Female
- Humans
- Hypertension
(drug therapy)
- Male
- Middle Aged
- Single-Blind Method
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