跳至主要内容
临床试验/JPRN-jRCT2080222155
JPRN-jRCT2080222155未知3 期

Phase III clinical study of DQ-2466 -Double-blind controlled study of fixed-dose and up-titration DQ-2466 regimens in subjects with persistent or permanent atrial fibrillation

DAIICHISANKYO Co.,Ltd.0 个研究点目标入组 120 人开始时间: 2013年7月26日最近更新:
适应症

试验速览

阶段
3 期
发起方
入组人数
120

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 20age old 至 ot applicable(—)
性别
All

入选标准

  • Patients who are diagnosed as persistent or permanent atrial fibrillation and have excessive mean heart rate above 80 beats per minute on Holter ECG.

排除标准

  • .Patients who recently took a beta-blocker or a calcium antagonist (e.g., diltiazem or verapamil)
  • .Patients receiving treatment for heart failure (NYHA classes II to IV).
  • .Patients with contraindication of carvedilol therapy.
  • .Patients with poorly controlled diabetes mellitus or hypertension.
  • .Patients with hepatic or renal impairment.

研究者

发起方
DAIICHISANKYO Co.,Ltd.

相似试验