跳至主要内容
临床试验/EUCTR2006-005804-15-IT
EUCTR2006-005804-15-IT进行中(未招募)不适用

Randomized double blind trial to evaluate the efficacy and safety of dronedarone (400 mg BID) versus amiodarone (600 mg daily for 28 days then 200 mg daily thereafter) for at least 6 months for the maintenance of sinus rhythm in patients with atrial fibrillation (AF - DIONYSIOS

sanofi-aventis recherche & de'veloppement0 个研究点目标入组 472 人开始时间: 2007年6月7日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
472

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Patients with documented AF for more than 72 hours for whom cardioversion and antiarrhythmic treatment is indicated in the opinion of the Investigator and receiving anticoagulants
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Patients aged below 21 years, - Contraindication to oral anticoagulation, - Patient having received amiodarone in the past whatever the date (more than a total of twenty 200 mg tablets or more than 5 days intravenous [IV]), - Women of childbearing potential without adequate birthcontrol; pregnant women; breastfeeding women, - History of torsades de pointes; family history of sudden cardiac death below age 50 years in the absence of coronary heart disease, - History of high degree atrio-ventricular block (2nd degree Mobitz 2 or higher), or significant sinus node disease (documented pause of 3 sec or more) without a permanent pacemaker implanted, - Bradycardia < 50 beats per minute (bpm) on the last 12-lead electrocardiogram (ECG) before randomization, - Clinically overt congestive heart failure with New-York Heart Association (NYHA) class III or IV at the time of randomization, - Ongoing potentially dangerous symptoms when in AF such as angina pectoris, transient ischemic attacks, stroke, syncope, as judged by the investigator, - Patients known to have chronic AF defined as continuous AF for more than 12 months, - Wolff-Parkinson-White Syndrome, - Patients with atrial flutter; patients with paroxysmal AF, - Hyperthyroidism; hypothyroidism, - Treatment with other Class I or III antiarrhythmic drugs

研究者

发起方
sanofi-aventis recherche & de'veloppement

相似试验

进行中(未招募)
不适用
Randomized double blind trial to evaluate the efficacy and safety of dronedarone (400 mg BID) versus amiodarone (600 mg daily for 28 days then 200 mg daily thereafter) for at least 6 months for the maintenance of sinus rhythm in patients with atrial fibrillation (AF) - DIONYSOSAtrial Fibrillation
EUCTR2006-005804-15-BEsanofi-aventis recherche & développement472
进行中(未招募)
不适用
Randomized double blind trial to evaluate the efficacy and safety of dronedarone (400 mg BID) versus amiodarone (600 mg daily for 28 days then 200 mg daily thereafter) for at least 6 months for the maintenance of sinus rhythm in patients with atrial fibrillation (AF) - DIONYSOSMedDRA version: 9.1Level: LLTClassification code 10003658Term: Atrial fibrillationAtrial Fibrillation
EUCTR2006-005804-15-DEsanofi-aventis recherche & développement472
进行中(未招募)
不适用
Randomized double blind trial to evaluate the efficacy and safety of dronedarone (400 mg BID) versus amiodarone (600 mg daily for 28 days then 200 mg daily thereafter) for at least 6 months for the maintenance of sinus rhythm in patients with atrial fibrillation (AF) - DIONYSOSMedDRA version: 9.1Level: LLTClassification code 10003658Term: Atrial fibrillationAtrial Fibrillation
EUCTR2006-005804-15-CZsanofi-aventis recherche & développement472
进行中(未招募)
1 期
Randomized double blind trial to evaluate the efficacy and safety of dronedarone (400 mg BID) versus amiodarone (600 mg daily for 28 days then 200 mg daily thereafter) for at least 6 months for the maintenance of sinus rhythm in patients with atrial fibrillation (AF) - DIONYSOSMedDRA version: 9.1Level: LLTClassification code 10003658Term: Atrial fibrillationAtrial Fibrillation
EUCTR2006-005804-15-PLsanofi-aventis recherche & développement472
进行中(未招募)
不适用
Randomized double blind trial to evaluate the efficacy and safety of dronedarone (400 mg BID) versus amiodarone (600 mg daily for 28 days then 200 mg daily thereafter) for at least 6 months for the maintenance of sinus rhythm in patients with atrial fibrillation (AF) - DIONYSOSAtrial Fibrillation
EUCTR2006-005804-15-FIsanofi-aventis recherche & développement472