NCT01426594Unknown不适用
Real-life Experience of the Use of Isomers as METPURE XL (S (-) Metoprolol Succinate) for Evaluation of Efficacy, Safety and Tolerability in the Management of Cardiovascular Disease in Colombian Patients
Closter Pharma1 个研究点 分布在 1 个国家目标入组 2,000 人开始时间: 2011年8月最近更新:
适应症
试验速览
- 阶段
- 不适用
- 发起方
- 入组人数
- 2,000
- 试验地点
- 1
- 主要终点
- Effect of therapy in the management of cardiovascular diseases
研究概览
简要总结
This is a Phase 4, observational, open study in patients who their doctor has prescribe METPURE XL (S (-)metoprolol succinate)by clinical practice. No medication was provided by the sponsor. The planned observation time is 8 weeks. The 8 weeks of observation involves an evaluation of baseline followed by information gathered from the assessment visits at week 4 and week 8.
研究设计
- 研究类型
- Observational
- 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
- •Patients who were prescibed with s(-)metoprolol succinate(25mg, 50mg), depending on their clinical condition and use locally approved will be eligible to participate in this study
排除标准
- 未提供
结局指标
主要结局
Effect of therapy in the management of cardiovascular diseases
时间窗: 8 weeks
The objective is to mesure the effect of Metpure XL in cadiovascular diseases as hypertension, post MI and coronary disease
次要结局
- Evaluate and compare the rate of compliance with treatment(8 weeks)
- Number of Participants with Adverse Events as a Measure of Safety and Tolerability(8 weeks)
研究者
研究点 (1)
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