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OpenTrials
Completed

NCT Number: NCT01956006

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

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.

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Key information

Age range

18 year–85 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

Alfred Hospital

Melbourne, Victoria, 3004, Australia

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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

Exclusion criteria

  • 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

Treatment and study plan

Milrinone

Drug

Administration of study medications, PK sampling and safety profile- add on haemodynamic invasive measurements if patient consents to.

Primary outcomes

  1. Safety and tolerability

    Time frame: 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)

Secondary outcomes

  1. NYHA Class

    Time frame: 3 months

    Change in Heart Failure Status

Other outcomes

  1. 6 minute walk test

    Time frame: 3 month

    Change in exercise capacity

  2. BNP

    Time frame: 3 month

  3. Number of Heart Failure Hospitalisation

    Time frame: 3 months

Sponsors and collaborators

Lead sponsor

The Alfred

Other

Registry information

Important dates

Study start
2013
Primary completion
2017
Study completion
2018
First posted
Oct 8, 2013
Registry last updated
Jan 11, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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