NCT07784296招募中不适用
A Multicenter, Prospective, Non-interventional, Observational Study to Evaluate Effectiveness and Safety of Sequential Triple Combination Therapy (Amlodipine/Losartan/Chlorthalidone) in Korean Patients With Hypertension
Hanmi Pharmaceutical Company Limited1 个研究点 分布在 1 个国家目标入组 3,500 人开始时间: 2026年3月19日最近更新:
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 3,500
- 试验地点
- 1
- 主要终点
- The change in Systolic Blood Pressure (SBP) relative to baseline
研究概览
简要总结
A multicenter, prospective, non-interventional, observational study to evaluate effectiveness and safety of sequential triple combination therapy (amlodipine/losartan/chlorthalidone) in Korean patients with hypertension
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Korean patients aged 19 years or older diagnosed with hypertension
- •Individuals newly diagnosed with hypertension or currently taking a single antihypertensive drug
- •Individuals for whom administration of Amoprel tablets has been determined based on the researcher's medical judgment
- •Individuals who have heard an explanation of this study and have voluntarily given written consent to participate in the study
排除标准
- •Individuals falling under the contraindications listed in the precautions for use of Amoprel Tab. or Amozartan Plus Tab.
- •Pregnant women, women who may be pregnant, and nursing mothers
- •Individuals currently participating in an interventional study
- •Individuals deemed unsuitable for participation in this study by the researcher for other reasons
结局指标
主要结局
The change in Systolic Blood Pressure (SBP) relative to baseline
时间窗: the 6-month time
次要结局
- effectiveness of sequential triple combination therapy (amlodipine/losartan/chlorthalidone)(2, 4, 6 months)
- Prescription patterns of a triple-therapy-based stepwise treatment strategy(2, 4, 6 months)
- safety of sequential triple combination therapy (amlodipine/losartan/chlorthalidone)(2, 4 , 6 months)
研究者
研究点 (1)
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