Advanced Chronic Heart FailurePhase 3ELEVATENCT01290146
ELEVATE Early LEvosimendan Vs Usual Care in Advanced Chronic hearT failurE
A Phase 3 study testing Diuretics and Levosimendan in people with Advanced Chronic Heart Failure, run by Niguarda Hospital at 22 sites in Italy.
Trial summary
The purpose of this study is to compare in patients with Advanced Chronic Heart Failure the effects of Levosimendan versus diuretic (single 24-hour infusion) applied at the early detection of impending destabilization on hospitalization-free survival during 12 months. Read more about this study
- Who is it for?
- Ages 18 to 80 years
- Conditions the study is for
- Advanced Chronic Heart Failure
- What is being tested?
- Diuretics and Levosimendan
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 13 participants
- Where
- 22 sitesItaly
- Study dates
- Feb 2011to Mar 2017
- Phase
- Phase 3
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 80 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Written informed consent
- Systolic dysfunction (LVEF ≤ 35% by echo assessment within 6 months before enrolment)
- No requirement for hospital admission for diagnostic work up or elective treatment to define etiology and/or treatment plan
- Already on optimal standard HF treatment based on individual tolerance, including cardiac resynchronization therapy (CRT)/ICD device according to current guidelines
- At least 2 hospital admissions for HF in the 6 months before enrolment, the most recent one within 30-90 days before enrolment with requirement for inotrope administration
Who cannot join
- Participant in other studies in the last 30 days
- Life expectancy < 1 year for comorbid conditions other than HF
- Pregnancy, lactation, childbearing potential unless on adequate contraception
- Acute coronary syndromes, percutaneous or surgical revascularization, valve surgery performed within 8 weeks before enrolment
- Planned percutaneous or surgical procedures (except for heart transplantation)
- CRT within 6 months before enrolment
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- Cardiogenic shock
- Supine systolic BP < 85 mmHg
- Severe liver insufficiency (>three-fold increase in AST-ALT )
- Sever chronic kidney dysfunction (estimated GFR < 30 ml/min)
- Sustained ventricular tachycardia
- Severe chronic or current acute infection (temperature >38 C, WBC >15,000/mm3)
- Severe chronic obstructive pulmonary disease (FEV1 <30% predicted or on oxygen therapy)
- Severe persistent anemia (Hb < 10 g/l))
- ACHF exacerbation due to conditions requiring specific treatment (e.g. anemia, atrial fibrillation, supraventricular tachycardia ) Documented low compliance or unavailable for programmed follow-up visits and phone contact
Trial locations and contacts
22 sites in 1 country.
22 sites in 1 country
Italy22 sites
Ospedali Riuniti di Ancona Cardiology Presidio Lancisi
Ancona, Ancona, 60020
Azienda Ospedaliero-Universitaria, Consorziale Policlinico di Bari, U.O. Cardiologia Universitaria, Dipartimento Emergenza e Trapianti di Organi
Bari, Bari
Ospedali Riuniti di Bergamo Cardiovascular Medicine
Bergamo, Bergamo, 24128
Ospedale Brotzu Cardiology
Cagliari, Cagliari, 09134
Fondazione S. Maugeri. IRCCS Istituto di Cassano Murge
Cassano Murge, Bari, 70020
Ospedale Sant'Anna Cardiology
Como, Como, 22100
Ospedale SS Annunziata Cardiology
Cosenza, Cosenza, 87100
Istituti Ospitalieri di Cremona Cardiology
Cremona, Cremona, 26100
Ospedale Santa Maria Nuova Cardiology
Florence, Firenze, 50100
Ospedale Vito Fazzi
Lecce, Lecce, 73199
Istituto Auxologico Italiano - IRCCS Clinical Cardiology Cardiovascular Department
Milan, Milan, 20148
Azienda Ospedaliera Niguarda Heart Failure and Heart Transplant Program
Milan, Milan, 20162
Azienda Ospedaliera S. Gerardo Hear Failure and Cardiomyopathy Clinic
Monza, Monza, 20052
Gruppo Policlinico di Monza Clinical Cardiology and Heart Failure Unit Cardiology Department
Monza, Monza, 20052
Ospedale Santa Maria della Misericordia Cardiology
Perugia, Perugia, 06156
Ospedale Guglielmo da Saliceto Cardiology Department
Piacenza, Piacenza, 29100
Azienda Ospedaliera San Camillo-Forlanini, Cardiology, Heart Failure Clinic
Roma, Roma, 00151
Università di Roma Sapienza Dipartimento di Scienze Cardiovascolari e Respiratorie
Roma, Roma, 00161
Azienda Ospedaliera San Giovanni- Addolorata 1st Cardiology Unit
Roma, Roma, 00184
Ospedale Santo Spirito, Cardiology
Roma, Roma, 00193
Azienda Ospedaliero-Universitaria, Ospedale di Cattinara Cardiology
Trieste, Trieste, 34149
Ospedale di Circolo e Fondazione Macchi Cardiology
Varese, Varese, 21100
About this study
Official title: Early Use of Levosimendan Compared to Usual Care in Advanced Chronic Heart Failure (ACHF)
The purpose of this study is to compare in patients with Advanced Chronic Heart Failure the effects of Levosimendan versus diuretic (single 24-hour infusion) applied at the early detection of impending destabilization on hospitalization-free survival during 12 months.
Patients with advanced chronic heart failure (ACHF) have a short term reduced life expectancy with recurrent hospital admissions for clinical exacerbations. Levosimendan improves contractility by calcium-dependent binding to troponin C, determines vasodilation of the coronary arteries and systemic resistance vessels, thus decreasing preload and afterload, while exerting a protective effect on the myocardium against ischemia-reperfusion damage. In randomized clinical trials of acute heart failure patients, levosimendan improved hemodynamics and patients' quality of life and decreased natriuretic peptide plasma levels, with no excess mortality The study will assess whether the administration of levosimendan (single 24-hour infusion) at the early detection of deterioration may reduce frequency and duration of hospital admissions, improve functional status and quality of life in ACHF patients, with respect to diuretic infusion.
Read the detailed description
BACKGROUND Patients with advanced chronic heart failure (ACHF) have a short term reduced life expectancy with recurrent hospital admissions for clinical exacerbations. ACHF poses a heavy burden to cardiology departments, where these patients are referred for the severity of their clinical condition, which require a specialist approach, and results in high health care costs due to frequent rehospitalizations.
Patients with ACHF ≥ 2 hospital admissions in 6 months are at high risk of recurrent exacerbations. The benefits of strict outpatient follow-up at specialised HF vs standard community care in ACHF patients have been consistently demonstrated. The standard approach at HF clinics is based on flexible diuretic dose and outpatient iv diuretics as bolus or infusion at early signs of decompensation. Although this strategy results in symptomatic benefit and prevents approximately one third of hospital admission for acute exacerbations, a relevant proportion of patients will still need hospitalization. Predictors of lack of benefit are low systolic blood pressure, prior increase in oral diuretics and beta-blocker use, which taken together represent markers of severe disease susceptible to evolve in a low output state.
In the HF clinic setting, a novel strategy for these patients, to include early support to myocardial contractility, i.e. before compelling criteria for hospital admission become manifest, might prevent further prolonged hospitalizations, myocardial damage and impairment in renal function TRIAL RATIONALE Levosimendan improved hemodynamics and patients' quality of life and decreased natriuretic peptide plasma levels, with no excess mortality, in randomized clinical trials of acute heart failure. In SURVIVE an early larger treatment effect of levosimendan was apparent in patients with acute worsening of chronic HF treatment than in those with de novo disease, possibly because a greater proportion of these patients may be on beta-blockers, that are known to interfere with dobutamine or may potentiate the circulatory actions of levosimendan. Thus levosimendan may be unattractive first-line agent in destabilized ACHF patients on beta-blockers.
Based on the drug cardioprotective properties, hemodynamic and neurohormonal effects, we propose a novel therapeutic approach for the clinically-driven use of levosimendan in recurrent acute exacerbations of ACHF.
Dosing of the drug will omit the bolus to increase tolerability in this severely ill patient population.
- Conditions
- Advanced Chronic Heart Failure
- Being tested
- Diuretics, Levosimendan
- Keywords
- Heart Failure, Levosimendan, Inotropic agents, Phosphodiesterase Inhibitors, Vasodilators, Diuretics
- Medical subject headings
- Heart Failure
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
DiureticsDrug
Patients randomized to diuretics receive a 24-hour diuretic infusion with a maximum cumulative dose up to 200 mg furosemide/24 h
LevosimendanDrug
Patients randomized to Levosimendan receive a 24-hour levosimendan infusion with NO prior bolus injection.
Starting doses will be based on baseline SBP levels
- SBP ≥ 85-99mmHg: 0.05 mcg/kg/min
- SBP ≥100 mmHg: 0.1 mcg/kg/min
| Study group | Role | What they receive |
|---|---|---|
| Diuretics | Active comparator | Patients randomized to diuretics receive a 24-hour diuretic infusion with a maximum cumulative dose up to 200 mg furosemide/24 h Receives: Drug: Diuretics |
| Levosimendan | Experimental | Patients randomized to Levosimendan receive a 24-hour levosimendan infusion with NO prior bolus injection.
Starting doses will be based on baseline SBP levels
* SBP ≥ 85-99mmHg: 0.05 mcg/kg/min
* SBP ≥100 mmHg: 0.1 mcg/kg/min Receives: Drug: Levosimendan |
What is being measured
The primary outcome is the main question the study is designed to answer.
Number of days alive free of Transplant and out-of-hospital (DAOH)
Measured: Measured at 12 months
Secondary outcomes (8)
Incidence of acute renal dysfunction
proportion of subjects who develop AKIN stage 1 (increase > 0.3 mg/dl or > 25% in serum creatinine from previous visit)
Measured: Measured at at 24 hours since inception of randomized treatment for acute worsening HF
All cause mortality, hospital readmission and unscheduled office and emergency department visits for ADCHF
A combination of all cause hospital admissions/death/urgent heart transplantation/LV assist device implantation
Measured: Measured at 12 months
BNP changes
Percent changes in BNP vs baseline
Measured: Measured at at end-of- study and at each eventual destabilization
Number of hospital admissions for acute worsening HF
Number of hospital admissions for acute worsening HF
Measured: Measured at 12 months
Costs
Direct health care costs for days in hospital, supplementary visits, drug treatment
Measured: Measured at 12 months
Treatment-related adverse events
death, hospital a dimission, emergency room or clinic unscheduled visits
Measured: Measured at 12 months
Adverse changes in blood pressure or heart rate
Hypotension (< 90 mmHg), tachycardia (> 110 bpm)
Measured: Measured at 24 hours after iv treatment
ECG changes
Rhythm, rate, conduction disturbances, ventricular arrhythmias, repolarization changes
Measured: Measured at 24 hours after iv treatment
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted4 Feb 2011 (estimated)
- Study startFeb 2011
- Primary completionJun 2015
- Study completionMar 2017
Why it stopped: Due to lack of enrollment
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Advanced Chronic Heart FailureStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 3
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 13 participants (actual)
Sponsor and investigators
- Lead sponsor
- Niguarda Hospital
- Sponsor type
- University, hospital or other
- Collaborators
- Orion Corporation, Orion Pharma
- Responsible party
- Sponsor
- Investigators
- Fabrizio Oliva, MD, Study chair, Heart Failure Heart Transplant Program, Cardiovascular Department, Niguarda Hospital, Milan, ItalyMichele Senni, MD, Study chair, Cardiovascular Medicine Ospedali Riuniti, Bergamo, Italy
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01290146
- Sponsor's protocol ID
- EudraCT code 2009-016958-41
- Other IDs
- FO002
- Acronym
- ELEVATE
- Status last verified
- Apr 2017
- First submitted
- 3 Feb 2011
- Last updated
- 10 Apr 2017
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 10 Apr 2017. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Early Use of Levosimendan Compared to Usual Care in Advanced Chronic Heart Failure (ACHF)
- ClinicalTrials.gov ID
- NCT01290146
- Acronym / sponsor ID
- ELEVATE / EudraCT code 2009-016958-41
- Conditions
- Advanced Chronic Heart Failure
- Keywords
- Heart Failure, Levosimendan, Inotropic agents, Phosphodiesterase Inhibitors, Vasodilators, Diuretics
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- TerminatedReason stopped: Due to lack of enrollment
- Enrolment
- 13 participants (actual)
- Lead sponsor
- Niguarda HospitalUniversity, hospital or other
- Collaborators
- Orion Corporation, Orion Pharma
- Study start
- Feb 2011 (actual)
- Primary completion
- Jun 2015 (actual)
- Study completion
- Mar 2017 (actual)
- First posted
- 4 Feb 2011 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The purpose of this study is to compare in patients with Advanced Chronic Heart Failure the effects of Levosimendan versus diuretic (single 24-hour infusion) applied at the early detection of impending destabilization on hospitalization-free survival during 12 months.
Patients with advanced chronic heart failure (ACHF) have a short term reduced life expectancy with recurrent hospital admissions for clinical exacerbations. Levosimendan improves contractility by calcium-dependent binding to troponin C, determines vasodilation of the coronary arteries and systemic resistance vessels, thus decreasing preload and afterload, while exerting a protective effect on the myocardium against ischemia-reperfusion damage. In randomized clinical trials of acute heart failure patients, levosimendan improved hemodynamics and patients' quality of life and decreased natriuretic peptide plasma levels, with no excess mortality The study will assess whether the administration of levosimendan (single 24-hour infusion) at the early detection of deterioration may reduce frequency and duration of hospital admissions, improve functional status and quality of life in ACHF patients, with respect to diuretic infusion.
Detailed description
BACKGROUND Patients with advanced chronic heart failure (ACHF) have a short term reduced life expectancy with recurrent hospital admissions for clinical exacerbations. ACHF poses a heavy burden to cardiology departments, where these patients are referred for the severity of their clinical condition, which require a specialist approach, and results in high health care costs due to frequent rehospitalizations.
Patients with ACHF ≥ 2 hospital admissions in 6 months are at high risk of recurrent exacerbations. The benefits of strict outpatient follow-up at specialised HF vs standard community care in ACHF patients have been consistently demonstrated. The standard approach at HF clinics is based on flexible diuretic dose and outpatient iv diuretics as bolus or infusion at early signs of decompensation. Although this strategy results in symptomatic benefit and prevents approximately one third of hospital admission for acute exacerbations, a relevant proportion of patients will still need hospitalization. Predictors of lack of benefit are low systolic blood pressure, prior increase in oral diuretics and beta-blocker use, which taken together represent markers of severe disease susceptible to evolve in a low output state.
In the HF clinic setting, a novel strategy for these patients, to include early support to myocardial contractility, i.e. before compelling criteria for hospital admission become manifest, might prevent further prolonged hospitalizations, myocardial damage and impairment in renal function TRIAL RATIONALE Levosimendan improved hemodynamics and patients' quality of life and decreased natriuretic peptide plasma levels, with no excess mortality, in randomized clinical trials of acute heart failure. In SURVIVE an early larger treatment effect of levosimendan was apparent in patients with acute worsening of chronic HF treatment than in those with de novo disease, possibly because a greater proportion of these patients may be on beta-blockers, that are known to interfere with dobutamine or may potentiate the circulatory actions of levosimendan. Thus levosimendan may be unattractive first-line agent in destabilized ACHF patients on beta-blockers.
Based on the drug cardioprotective properties, hemodynamic and neurohormonal effects, we propose a novel therapeutic approach for the clinically-driven use of levosimendan in recurrent acute exacerbations of ACHF.
Dosing of the drug will omit the bolus to increase tolerability in this severely ill patient population.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Diuretics | Active comparator | Drug: DiureticsPatients randomized to diuretics receive a 24-hour diuretic infusion with a maximum cumulative dose up to 200 mg furosemide/24 h |
| Levosimendan | Experimental | Drug: LevosimendanPatients randomized to Levosimendan receive a 24-hour levosimendan infusion with NO prior bolus injection. Starting doses will be based on baseline SBP levels * SBP ≥ 85-99mmHg: 0.05 mcg/kg/min * SBP ≥100 mmHg: 0.1 mcg/kg/min |
Who may qualify
- Ages
- 18 to 80 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (5 listed)
- Written informed consent
- Systolic dysfunction (LVEF ≤ 35% by echo assessment within 6 months before enrolment)
- No requirement for hospital admission for diagnostic work up or elective treatment to define etiology and/or treatment plan
- Already on optimal standard HF treatment based on individual tolerance, including cardiac resynchronization therapy (CRT)/ICD device according to current guidelines
- At least 2 hospital admissions for HF in the 6 months before enrolment, the most recent one within 30-90 days before enrolment with requirement for inotrope administration
Key exclusion criteria (15 listed)
- Participant in other studies in the last 30 days
- Life expectancy < 1 year for comorbid conditions other than HF
- Pregnancy, lactation, childbearing potential unless on adequate contraception
- Acute coronary syndromes, percutaneous or surgical revascularization, valve surgery performed within 8 weeks before enrolment
- Planned percutaneous or surgical procedures (except for heart transplantation)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| DiureticsPatients randomized to diuretics receive a 24-hour diuretic infusion with a maximum cumulative dose up to 200 mg furosemide/24 h | Drug | Diuretics |
| LevosimendanPatients randomized to Levosimendan receive a 24-hour levosimendan infusion with NO prior bolus injection. Starting doses will be based on baseline SBP levels * SBP ≥ 85-99mmHg: 0.05 mcg/kg/min * SBP ≥100 mmHg: 0.1 mcg/kg/min | Drug | Levosimendan |
Primary outcome
Number of days alive free of Transplant and out-of-hospital (DAOH)
Time frame: Measured at 12 months
8 secondary outcomes
Incidence of acute renal dysfunction
Time frame: Measured at at 24 hours since inception of randomized treatment for acute worsening HF
All cause mortality, hospital readmission and unscheduled office and emergency department visits for ADCHF
Time frame: Measured at 12 months
BNP changes
Time frame: Measured at at end-of- study and at each eventual destabilization
Number of hospital admissions for acute worsening HF
Time frame: Measured at 12 months
Costs
Time frame: Measured at 12 months
Treatment-related adverse events
Time frame: Measured at 12 months
Adverse changes in blood pressure or heart rate
Time frame: Measured at 24 hours after iv treatment
ECG changes
Time frame: Measured at 24 hours after iv treatment
Results and safety
The study was stopped early (reason given: Due to lack of enrollment). Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 10 Apr 2017.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Fabrizio Oliva, MD study chair
Heart Failure Heart Transplant Program, Cardiovascular Department, Niguarda Hospital, Milan, Italy
Michele Senni, MD study chair
Cardiovascular Medicine Ospedali Riuniti, Bergamo, Italy
22 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing Diuretics and Levosimendan in people with Advanced Chronic Heart Failure, run by Niguarda Hospital at 22 sites in Italy.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 15 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: stopped early, as of the sponsor's last update on 10 Apr 2017. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 22 sites in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study was stopped early (reason given: Due to lack of enrollment). Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Number of days alive free of Transplant and out-of-hospital (DAOH) (time frame: Measured at 12 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Apr 2017.