NCT02235415已完成不适用
Observation of the Efficacy and Tolerance of Motens® (Lacidipine) in Patients With Essential Hypertension, Under Normal Conditions Compared With an Open Clinical Trial
适应症
干预措施
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 24,526
- 主要终点
- Assessment of efficacy by the investigator on a 4-point verbal rating scale based on changes in blood pressure
研究概览
简要总结
Study of the efficacy and tolerance of Motens® (lacidipine) in patients with essential hypertension. To obtain information on the dosage used in practice and the tolerance at the start of treatment (12 weeks)
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Non-hospitalised patients of both sexes aged 18 years or more with essential hypertension requiring treatment according to the recommendations of the German League for Hypertension
排除标准
- •Patients who had the contraindications listed in the product information (the case report file contained a copy of the product information)
研究组 & 干预措施
Motens
干预措施: Motens® (lacidipine) (Drug)
结局指标
主要结局
Assessment of efficacy by the investigator on a 4-point verbal rating scale based on changes in blood pressure
时间窗: Up to 12 weeks after start of drug administration
Number of patients with adverse events
时间窗: Up to 12 weeks after start of drug administration
Assessment of tolerability by investigator on a 4-point verbal rating scale
时间窗: Up to 12 weeks after start of drug administration
次要结局
未报告次要终点
研究者
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