Effect of Ivabradine in Stage D HF/Cardiogenic Shock Patients on Dobutamine
Effect of Ivabradine on Heart Rate and Hemodynamics in Patients With Stage D Heart Failure (HF)/Cardiogenic Shock on Dobutamine Treatment
1 other identifier
interventional
40
1 country
1
Brief Summary
This is a randomized, double blind, single center trial to study of the effects of Ivabradine vs. Placebo on patients hospitalized for Stage D heart failure (HF)/ and cardiogenic shock (CS) who will require continuous infusion of Dobutamine and have developed sinus tachycardia (ST) (heart rate \>100 beats/min). The aim of the study will be to assess the potential of Ivabradine to slow ST and improve hemodynamics in patients with stage D HF/CS on Dobutamine treatment.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for phase_4 heart-failure
Started Mar 2018
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 15, 2017
CompletedFirst Posted
Study publicly available on registry
January 2, 2018
CompletedStudy Start
First participant enrolled
March 15, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2020
CompletedMay 23, 2019
May 1, 2019
1.8 years
December 15, 2017
May 21, 2019
Conditions
Outcome Measures
Primary Outcomes (1)
Heart rate
Heart rate will be measured and any changes noted
72 hours
Secondary Outcomes (2)
cardiac index
72 hours
plasma brain natriuretic peptide (BNP) level
72 hours
Study Arms (2)
Ivabradine
ACTIVE COMPARATORInitiation at dose 5 mg PO x 1 dose and further increased in 12 hours to 7.5 mg PO twice per day if patient is stable with mean BP≥ 60 mmHg, systolic blood pressure ≥ 90 mmHg and HR ≥100 bpm
Placebo
PLACEBO COMPARATORMatching placebo given PO twice per day
Interventions
ivabradine or placebo given orally 2 times daily for 72 hours
Eligibility Criteria
You may qualify if:
- Provide written informed consent for the study
- Have current diagnosis of Ischemic and/or non-ischemic cardiomyopathy
- Left ventricular ejection fraction (LVEF) \< 30% by echo during the screening
- Sinus rhythm with HR ≥100 bpm
- Systolic blood pressure ≥ 90 mmHg assessed by cuff sphygmomanometer
- CI \< 2.2 L/min/m2
- Current symptom(s) of HF (New York Heart Association (NYHA) class IV) at Screening.
- Absence of hypovolemia, defined as a central venous pressure ≥10 mmHg and pulmonary capillary occlusion pressure ≥15 mmHg before administration of Dobutamine
You may not qualify if:
- Respiratory support with mechanical ventilation
- Circulatory mechanical support
- Atrial pacing with the presence of sick sinus syndrome or sino-atrial block
- Second or third degree atrioventricular (AV) block,
- Atrial fibrillation/flutter
- Amiodarone treatment
- Ventricular tachycardia
- Acute coronary syndrome
- Bilirubin \> 2.5
- Alanine aminotransferase (ALT) \>60 IE/L,
- Serum creatinine \>2.5 g/ml)
- Fever and significant infection
- Pregnancy
- Anemia, Hgb \< 9.0
- Patients required treated with severe cytochrome CYP3A4 inhibitors drugs Concomitant use of strong CYP3A4 inhibitors will be avoided during the study period
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Loyola Universitylead
- Amgencollaborator
Study Sites (1)
Loyola University Medical Center
Maywood, Illinois, 60153, United States
Related Publications (27)
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PMID: 19559207BACKGROUNDDiFrancesco D, Camm JA. Heart rate lowering by specific and selective I(f) current inhibition with ivabradine: a new therapeutic perspective in cardiovascular disease. Drugs. 2004;64(16):1757-65. doi: 10.2165/00003495-200464160-00003.
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PMID: 18757088BACKGROUNDSwedberg K, Komajda M, Bohm M, Borer JS, Ford I, Dubost-Brama A, Lerebours G, Tavazzi L; SHIFT Investigators. Ivabradine and outcomes in chronic heart failure (SHIFT): a randomised placebo-controlled study. Lancet. 2010 Sep 11;376(9744):875-85. doi: 10.1016/S0140-6736(10)61198-1.
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PMID: 26967048BACKGROUNDTardif JC, O'Meara E, Komajda M, Bohm M, Borer JS, Ford I, Tavazzi L, Swedberg K; SHIFT Investigators. Effects of selective heart rate reduction with ivabradine on left ventricular remodelling and function: results from the SHIFT echocardiography substudy. Eur Heart J. 2011 Oct;32(20):2507-15. doi: 10.1093/eurheartj/ehr311. Epub 2011 Aug 29.
PMID: 21875858BACKGROUNDFang Y, Debunne M, Vercauteren M, Brakenhielm E, Richard V, Lallemand F, Henry JP, Mulder P, Thuillez C. Heart rate reduction induced by the if current inhibitor ivabradine improves diastolic function and attenuates cardiac tissue hypoxia. J Cardiovasc Pharmacol. 2012 Mar;59(3):260-7. doi: 10.1097/FJC.0b013e31823e5e01.
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PMID: 18313622BACKGROUND
Related Links
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Eugenia Raichlin, MD
Loyola University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- phase 4
- Allocation
- RANDOMIZED
- Masking
- TRIPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, INVESTIGATOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Professor
Study Record Dates
First Submitted
December 15, 2017
First Posted
January 2, 2018
Study Start
March 15, 2018
Primary Completion
January 1, 2020
Study Completion
June 1, 2020
Last Updated
May 23, 2019
Record last verified: 2019-05
Data Sharing
- IPD Sharing
- Will not share