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临床试验/NCT01956006
NCT01956006已完成1 期

Pilot Study of Slow Release Oral Milrinone in Patients With Advanced Heart Failure

The Alfred1 个研究点 分布在 1 个国家目标入组 26 人开始时间: 2013年10月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
26
试验地点
1
主要终点
Safety and tolerability

研究概览

简要总结

Advanced heart failure (HF), ineffective pumping of the heart, is a common, life-threatening cardiovascular disorder, characterised by marked symptomatic limitation and frequent hospitalization. It is particularly prevalent in older individuals (up to 10% of the population) and it has become the most common cause for hospitalization in people >65yrs. As such it is also one of the leading consumers of healthcare spending. Recurrent hospitalization is frequently due in significant part to the lack of viable therapeutic options for severe HF. During hospital admission, medications through a drip to give through a vein (intravenous therapy), is required to improve heart pumping capacity (such as milrinone).They are frequently used and in many cases prolonged treatment periods of intravenous therapy are required. In a growing number of cases, there is a need to continue this treatment at home, however this is particularly costly and often complicated by intravenous line infection. As such there is an expanding need for therapeutic options in patients with advanced HF. Over 20 years ago, studies of the potential utility of a rapid release form of oral milrinone were examined, however these studies demonstrated adverse effects due to its quick release.

This study aims to determine the safety and tolerability of slow release oral milrinone in advanced HF patients with no further clinical option and to evaluate its effects on HF status.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Advanced HF (current inpatients) with no further clinical options as defined by treating cardiologist.
  • NYHA III-IV
  • LVEF<35%
  • Recurrent hospitalization (>/=3 admissions in the preceding 12 months) for HF
  • On optimal tolerated medical/device therapy. Stable therapy for 48hrs.
  • Age 18-85 yrs
  • Provide written informed consent prior to any study procedure and agree to adhere to all protocol requirements

排除标准

  • Hypotension (BPsys<85)
  • Unstable rhythm including frequent non-sustained ventricular tachycardia or poorly controlled atrial fibrillation (ventricular rate >100).
  • Severe renal impairment Cr>250umol/L or dialysis.
  • Other life-threatening eg neoplastic, haematological, hepatic or pulmonary disease.
  • Pregnancy or female with childbearing potential and inability to use contraception

研究组 & 干预措施

MIlrinone

Experimental

ER milrinone

干预措施: Milrinone (Drug)

结局指标

主要结局

Safety and tolerability

时间窗: 3 months

Number of MACE events change from basline safety profile bloods (Full Blood Count, urea and creatine, Liver function counts) Change in haemodynamic measurements ECG and Blood pressure and HR Monitoring Swan Ganz insertion for haemodynamic measurements (RA volume , RVSP, CO, PA, PAWP)

次要结局

  • NYHA Class(3 months)

研究者

发起方
The Alfred
申办方类型
Other
责任方
Principal Investigator
主要研究者

Prof David Kaye

Head, Experimental Cardiology and Heart Failure Division Baker Heart Research Institute & Cardiologist, Heart Centre, Alfred Hospital

The Alfred

研究点 (1)

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Pilot Study of Slow Release Oral Milrinone in... | 临床试验