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临床试验/NCT03710057
NCT03710057已完成不适用

A Post-Marketing, Prospective, Observational Program: Effect of Ivabradrine in Lowering Heart Rate and Quality of Life in Chronic Heart Failure Patients

Getz Pharma0 个研究点目标入组 50 人开始时间: 2016年12月1日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
50
主要终点
Mean difference of Heart Rate

研究概览

简要总结

Elevated Heart rate (HR) (≥ 70 bpm) is one of the contributing factors in increasing the burden of hospitalization among Heart Failure patient. Ivabradine is a novel, selective and specific in inhibiting a Funny current in sinoatrial node Node and approved as an alternative therapy for Chronic Heart Failure (CHF) patients. CHF patients when treated with Ivabradine reported 39%, and 30% reduction in mortality and hospitalization rate respectively. Patient were treated with Ivabradine 5mg twice daily to determine its effect in lowering Heart rate and the Quality of Life (QOL) in Chronic Heart Failure patients

详细描述

A prospective, post-marketing observational study was conducted in 50 chronic heart failure patients with age 30-70yrs of NYHA Class II and prescribed 5 mg Ivabradine twice daily. Heart rate was evaluated through ECG & quality of life was measured by a validated questionnaire EuroQol-5 Dimension 3 level version (EQ-5D-3L). Baseline demographic includes age, gender, height, weight, Body Mass Index, temperature, blood pressure and respiratory rate were recorded and patients were followed at week 4 and week 8. Safety and tolerability was assessed by adverse drug reaction (ADR) monitoring. Results were analyzed by statistical software SPSS version 20.0.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
30 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Written informed consent
  • Known case of Chronic Heart Failure (New York Heart Association (NYHA) functional class II to III)
  • Clinically stability (at least for 4 weeks)
  • Resting heart rate of more than 70 beats/ min (bpm) as assessed from the 12-lead electrocardiogram.

排除标准

  • Hypersensitivity to the active substance or to any of the excipients
  • Resting heart rate below 70 beats per minute prior to treatment
  • Cardiogenic shock
  • Acute myocardial infarction
  • Severe hypotension (< 90/50 mmHg)
  • Severe hepatic insufficiency
  • Sick sinus syndrome
  • Sino-atrial block
  • Unstable or acute heart failure
  • Pacemaker dependent (heart rate imposed exclusively by the pacemaker)
  • Unstable angina
  • Atrioventricular Block of 3rd degree
  • The combination with a strong cytochrome P450 3A4 inhibitors such as azole antifungals (ketoconazole, itraconazole), macrolide antibiotics (clarithromycin, erythromycin, telithromycin), HIV protease inhibitors (nelfinavir, ritonavir) and nefazodone
  • The combination with verapamil or diltiazem which are moderate CYP3A4 inhibitors with heart rate reducing properties.
  • Pregnancy, lactation and women of child-bearing potential not using appropriate contraceptive measures

结局指标

主要结局

Mean difference of Heart Rate

时间窗: at 4 week and 8 week

The primary end-point was the overall response rate of patients to Ivabradine in achieving HR \<70 Bpm

次要结局

  • Percentage of problems reported in EQ-5D descriptive system(at 4 week and 8 week)
  • Median score of EQ-5D visual analogue scale(at 4 week and 8 week)

研究者

发起方
Getz Pharma
申办方类型
Industry
责任方
Principal Investigator
主要研究者

Dr. Fawad Farooq

Assistant Professor, Consultant Cardiologist

National Institute of Cardiovascular Diseases, Pakistan

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