JPRN-jRCT2031230283招募中Unknown
Special drug use surveillance of Entresto Tablets (Hypertension, CLCZ696A1402): ENLIGHT
Sugigmoto Toshiya0 个研究点目标入组 1,000 人开始时间: 2023年8月9日最近更新:
适应症
试验速览
- 阶段
- Unknown
- 状态
- 招募中
- 发起方
- 入组人数
- 1,000
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- ot applicable 至 ot applicable(—)
- 性别
- All
入选标准
- •1. Patients who have given written consent to participate in this study before the start of treatment with Entresto
- •2. Patients who used Entresto for the first time for the indication of hypertension
排除标准
- •1. Patients who have received a formulation containing the same ingredient as Entresto (including investigational product or post-marketing clinical study drug)
- •2. The following patients for whom administration of Entresto is contraindicated in the package insert:
- •-Patients with a history of hypersensitivity to any of the ingredients of Entresto
- •-Patients who are receiving angiotensin-converting enzyme inhibitors (alacepril, imidapril hydrochloride, enalapril maleate, captopril, quinapril hydrochloride, cilazapril hydrate, temocapril hydrochloride, delapril hydrochloride, trandolapril, benazepril hydrochloride, perindopril erbumine, and lisinopril hydrate) or who discontinued these drugs within 36 hours.
- •-Patients with a history of angioedema (angioedema due to angiotensin II receptor antagonists or angiotensin converting enzyme inhibitors, hereditary angioedema, acquired angioedema, idiopathic angioedema, etc.)
- •-Patients with diabetes mellitus who are receiving aliskiren fumarate
- •-Patients with severe hepatic impairment (Child-Pugh class C)
- •-Pregnant or possibly pregnant women
- •3. Patients with a history or complication of cardiac failure
- •4. Patients who have been hospitalized at the start of treatment with Entresto
研究者
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