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RecruitingNCT06884631MECKIUpdated Mar 19, 2025

Metabolic Exercise Test Data Combined with Cardiac and Kidney Indexes (MECKI) Score Evolution: Identification of Cardiovascular Risk in Patients with Heart Failure

An observational study in Heart Failure, sponsored by Centro Cardiologico Monzino. Recruiting at 26 sites in Italy. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-03-19.

Sponsored by Centro Cardiologico Monzino · Observational

From the registry’s dates

  • Started Feb 2021; still recruiting 5 years 7 months later.
Study type
Observational
Model
Cohort
Time perspective
Other
Enrollment
10,000
Ages
18 Years and older
Sex
All
01

Study summary

Heart failure is a complex condition involving multiple organs beyond the cardiovascular system, all influencing disease progression and prognosis. Accurate risk assessment requires considering multiple variables, as no single parameter alone provides a complete prognostic picture.

This has led to the development of prognostic models combining clinical and laboratory parameters. Some of these models incorporate cardiopulmonary exercise testing (CPET), which provides key prognostic indicators. Since the 1990s, CPET has been recommended in heart failure management guidelines due to its strong prognostic value when combined with clinical data.

However, existing risk models often exclude important predictors such as ventilatory parameters from CPET (VE/VCO₂), renal function, and hemoglobin levels. To address this gap, in 2012 the investigators developed the MECKI (Metabolic Exercise test data combined with Cardiac and Kidney Indexes) score, integrating oxygen consumption, ventilatory efficiency, and easily accessible biochemical and echocardiographic parameters. Unlike previous models requiring extensive data collection, MECKI is based on only six variables, making it practical and effective.

Recent studies suggest the need to update the cutoff values and parameters used for risk stratification, as new therapies and treatment strategies may significantly alter prognostic accuracy in different patient populations.

This study aims to expand and refine the MECKI score by updating the patient dataset, optimizing its performance in specific subgroups, and aligning it with emerging therapeutic approaches.

Additionally, the investigators will evaluate whether the model's risk accuracy varies in advanced-stage patients, those with comorbidities, or under different treatment regimens. This could lead to correction factors that enhance the score's predictive power across diverse clinical scenarios, further improving its applicability and reliability in heart failure management.

Read the detailed description

Heart failure is a complex condition affecting multiple organs beyond the cardiovascular system, influencing disease progression and prognosis. It has become increasingly evident that accurate risk assessment requires considering multiple variables, as no single parameter alone is sufficient for prognosis.

These findings have led to the identification and study of prognostic parameters that, when combined, allow for a more precise risk estimation and identification of high-risk patients. Various prognostic scores have been developed, utilizing algorithms that integrate multiple variables to estimate an individual's mortality risk. Some scores are based on clinical evaluation and comorbidities, others on laboratory findings, baroreflex sensitivity, heart rate, sleep abnormalities, echocardiographic imaging, or cardiopulmonary exercise testing (CPET), either alone or in combination with other factors.

CPET provides several parameters strongly correlated with prognosis. Since the 1990s, its use-alongside clinical data-has been recommended in heart failure management guidelines. More recently, in addition to peak oxygen consumption, the VE/VCO₂ slope has been recognized as a key prognostic marker, reflecting ventilatory efficiency and ventilation-perfusion mismatch, and has been included in heart transplant assessment criteria.

Current risk models in heart failure often omit important prognostic parameters, such as ventilatory indices from CPET, renal function, and hemoglobin levels. Among the numerous prognostic scores available, only the HF Survival Score (HFSS) and the HF Action Predictive Risk Score Model incorporate exercise-related parameters (peak VO₂ in the former and exercise duration in the latter), yet both neglect ventilatory aspects. Even the widely used Seattle Score does not include exercise-related variables.

In 2012, the researchers developed the MECKI (Metabolic Exercise test data combined with Cardiac and Kidney Indexes) score, integrating oxygen consumption, ventilatory efficiency, and easily accessible biochemical and echocardiographic parameters. Unlike previous models requiring extensive data collection, MECKI is based on just six key variables, making it both practical and effective.

Recent studies indicate the need to review and update the cutoff values and parameters used in prognostic models, as the introduction of new therapies and treatment strategies may significantly impact their predictive power in specific patient populations.

Study Objectives and Purpose The aim of this study is to expand and update the patient dataset to further develop the MECKI score, optimizing its application in patient subgroups and adapting it to new therapies and treatments introduced in clinical practice.

Additionally, the researchers seek to determine whether risk prediction accuracy varies in advanced-stage patients, those with comorbidities, or those receiving different treatments. This could lead to the development of correction factors for the MECKI score, improving its predictive power and applicability across different clinical scenarios.

Study Population Patients with systolic heart failure, consecutively enrolled and followed at multiple Heart Failure Units across Italy.

Patients undergo assessment through medical history collection, physical examination, laboratory tests, ECG, transthoracic echocardiography, and cardiopulmonary exercise testing (CPET).

Follow-up will be conducted according to the protocol of the respective Heart Failure Unit. The follow-up period ends at the last evaluation at the reference center, or upon the patient's death or heart transplantation.

02

Conditions studied

  • Heart Failure

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Keywords

  • prognosis
  • risk score
  • heart failure
  • cardiopulmonary exercise test
  • exercise
03

In context

Heart Failure

5,701 studies on the registry are indexed under Heart Failure; 1,220 are open to participants now.

This study's planned enrollment of 10,000 is above the median of 200 across 1,679 observational studies indexed under Heart Failure.

Browse Heart Failure studies →

Lead sponsor

Centro Cardiologico Monzino is the lead sponsor of 69 studies on the registry; 24 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Patients with past or present heart failure (with previous documentation of left ventricular systolic dysfunction (LVEF \<40%)), in stable clinical conditions, who underwent a cardiopulmonary exercise test, with no scheduled cardiovascular treatment.

Inclusion criteria

  • age >18 past or present heart failure (NYHA functional class I-III, stage C of the ACC/AHA classification)
  • documentation of left ventricular systolic dysfunction (LVEF \<40%)
  • stable clinical conditions
  • previous or concomitant cardiopulmonary exercise test

Exclusion criteria

Exclusion Criteria:

  • scheduled cardiovascular treatment
  • clinical unstable condition
  • History of pulmonary embolism, significant valvular disease, pericardial disease, severe COPD, exercise-induced angina, exercise-induced ECG changes, severe brady- or tachyarrhythmias, or the presence of comorbidities that interfere with exercise performance.
05

Study design

Observational model
Cohort
Time perspective
Other
Enrollment
10,000 participants (estimated)
Target follow-up
10 Years
Patient registry
Yes

Groups and cohorts

  • Heart failure patients

    Patients with systolic heart failure, able to exercise

06

What researchers measure

Primary outcomes

  1. Risk score

    Expand and update the patient dataset to further develop the Metabolic Exercise test data combined with Cardiac and Kidney Indexes (MECKI) score, optimizing its application in specific patient subgroups and aligning it with newly introduced therapies and treatments in clinical practice.

    Time frame: From enrollment to endpoint occurence (death, LVAD implantation, heart transplant) within 15 years

  2. End point

    Time to Cardiovascular death or LVAD implantation or heart transplant

    Time frame: From enrollment to endpoint occurence (death, LVAD implantation, heart transplant) within 15 years

07

Study locations

19 of 26 sites recruiting
  • Ospedali Riuniti di Ancona
    Ancona, Italy
    Recruiting
  • Istituti Clinici Scientifici Maugeri Bari
    Bari, Italy
    Recruiting
  • Ospedale papa Giovanni XXIII
    Bergamo, Italy
    Recruiting
  • Spedali Civili Brescia
    Brescia, Italy
    Not yet recruiting
  • Spedali Civili
    Brescia, Italy
    Recruiting
  • Università di Foggia
    Foggia, Italy
    Recruiting
  • Centro Cardiologico Monzino
    Milano, 20138, Italy
    Recruiting
  • I.R.C.C.S. Ospedale San Raffaele
    Milano, Italy
    Recruiting
  • IRCCS Istituto Auxologico Italiano
    Milano, Italy
    Recruiting
  • IRCCS Multimedica- Ospedale San Giuseppe
    Milano, Italy
    Recruiting
  • Istituti Clinici Scientifici Maugeri Milano
    Milano, Italy
    Not yet recruiting
  • Ospedale Cà Granda- A.O. Niguarda
    Milano, Italy
    Not yet recruiting
  • Federico II hospital
    Naples, Italy
    Recruiting
  • Azienda Ospedaliera dei Colli - Ospedale Monaldi
    Napoli, Italy
    Recruiting
  • Università degli Studi di Napoli Federico II
    Napoli, Italy
    Recruiting
  • Istituto Mediterraneo per i Trapianti e Terapie ad alta specializzazione
    Palermo, Italy
    Not yet recruiting
  • Ospedale Guglielmo da Saliceto
    Piacenza, Italy
    Recruiting
  • Fondazione Gabriele Monasterio
    Pisa, Italy
    Recruiting
  • Azienda Ospedaliera San Camillo-Forlanini
    Roma, Italy
    Recruiting
  • Azienda Ospedaliera Sant'Andrea
    Roma, Italy
    Recruiting
  • Azienda Ospedaliero-Universitaria Policinico Umberto I
    Rome, Italy
    Not yet recruiting
  • Santo Spirito Hospital
    Rome, Italy
    Recruiting
  • IRCCS Policlinico San Donato
    San Donato Milanese, Italy
    Recruiting
  • S. Maria alle Scotte Hospital UOC cardiologia clinico-chirurgica (UTIC)
    Siena, Italy
    Not yet recruiting
  • S. Maria alle Scotte Hospital UOSA malattie cardiovascolari
    Siena, Italy
    Not yet recruiting
  • Azienda sanitaria universitaria Giuliano Isontina (ASUGI)
    Trieste, Italy
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 19, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06884631
Lead sponsor
Centro Cardiologico Monzino
Collaborators
Santo Spirito Hospital, Italy, Fondazione Toscana Gabriele Monasterio, Spedali Civili, University of Brescia, Italy, Monaldi Hospital, Azienda Sanitaria Universitaria Giuliano Isontina (ASU GI), San Raffaele University Hospital, Italy, University of Foggia, Azienda Ospedaliera Niguarda Cà Granda, Azienda Policlinico Umberto I, Federico II University of Naples, Department of Clinical Medicine and Surgery, Naples, Italy, Città di Lecce Hospital, Policlinico G . Martino, Messina Italy, Azienda Ospedaliera Universitaria Senese, Azienda Sanitaria di Firenze, Ospedale San Luca, Istituto Auxologico Italiano, Milano, Casa di Cura Mater Dei, Policlinico Bari University Hospital (Bari, Italy), Azienda Ospedaliera di Perugia, I.R.C.C.S. Policlinico San Donato, San Donato Milanese, Italy, IRCCS Multimedica, Ospedali Riuniti Ancona, ASST Papa Giovanni XXIII, Bergamo, Italy, S. Andrea Hospital, Istituti Clinici Scientifici Maugeri SpA, Istituto Auxologico Italiano - IRCCS - Ospedale San Luca - Milano, Azienda Ospedaliero-Universitaria Senese, The Mediterranean Institute for Transplantation and Advanced Specialized Therapies, Federico II University, Ospedale Guglielmo da Saliceto, Piacenza
Responsible party
Piergiuseppe Agostoni (Professor, Centro Cardiologico Monzino) — Principal investigator
First posted
Mar 19, 2025
Start date
Feb 10, 2021
Primary completion
Dec 31, 2026 (estimated)
Completion
Dec 31, 2028 (estimated)
Last update
Mar 19, 2025

Study contacts

Piergiuseppe Agostoni, Professor
Contact
piergiuseppe.agostoni@ccfm.it
+390258002010
Elisabetta Salvioni, PhD
Contact
elisabetta.salvioni@ccfm.it
+390258002010

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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