AzTrials
AzTrials

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.

Terminated

Stopped early. The study ended before it was planned to and will not resume.

Official record
Search all trials

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
Show all 15Show fewer
  • 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

Other trials in Italy

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.

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 groups in NCT01290146
Study groupRoleWhat they receive
DiureticsActive comparatorPatients randomized to diuretics receive a 24-hour diuretic infusion with a maximum cumulative dose up to 200 mg furosemide/24 h
Receives: Drug: Diuretics
LevosimendanExperimentalPatients 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.

  1. Number of days alive free of Transplant and out-of-hospital (DAOH)

    Measured: Measured at 12 months

Secondary outcomes (8)
  1. 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

  2. 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

  3. BNP changes

    Percent changes in BNP vs baseline

    Measured: Measured at at end-of- study and at each eventual destabilization

  4. Number of hospital admissions for acute worsening HF

    Number of hospital admissions for acute worsening HF

    Measured: Measured at 12 months

  5. Costs

    Direct health care costs for days in hospital, supplementary visits, drug treatment

    Measured: Measured at 12 months

  6. Treatment-related adverse events

    death, hospital a dimission, emergency room or clinic unscheduled visits

    Measured: Measured at 12 months

  7. Adverse changes in blood pressure or heart rate

    Hypotension (< 90 mmHg), tachycardia (> 110 bpm)

    Measured: Measured at 24 hours after iv treatment

  8. 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.

  1. First posted4 Feb 2011 (estimated)
  2. Study startFeb 2011
  3. Primary completionJun 2015
  4. Study completionMar 2017

Why it stopped: Due to lack of enrollment

Resources

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)
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

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.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in