跳至主要内容
临床试验/JPRN-jRCT2031230283
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

发起方
Sugigmoto Toshiya

相似试验