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The Predictive Value of Dobutamine Echo-stress in the Clinical Response to CCM Therapy in Advanced HF
Sponsor: Quovadis Associazione
Summary
The goal of this observational cohort study, which is both retrospective and prospective, is to evaluate the long-term clinical and instrumental response to Cardiac Contractility Modulation (CCM) treatment in adult subjects suffering from symptomatic heart failure (HF) due to systolic left ventricular dysfunction, despite adequate medical therapy. Based on the response to stress echocardiography with preimplantation low-dose Dobutamine, the main questions it aims to answer are: * What is the proportion of subjects who experience a clinical response to CCM therapy at 12 months (NYHA reduction ≥ 1 class)? * There was a reduction in the number of hospitalizations, visits to the Emergency Department, and access to day hospital facilities for more than 4 hours compared to the year before the study (e.g., by intravenous infusion of cardiac inotropic drugs)? * What is the estimated change in the quality-of-life score using the "Quality of Life Questionnaire with Heart Failure - Minnesota" (MLHFQ) between baseline and the end of follow-up? * What is the change in walking distance between baseline and the end of the follow-up in the walk test (6MWT) (optional)? * What is the difference in NT-proBNP levels between baseline and the end of follow-up? Participants are already receiving CCM support as part of their regular medical care for heart failure.
Official title: Advanced Heart Failure: The Predictive Value of Dobutamine Echo-stress in the Clinical Response to Cardiac Contractility Modulation Therapy (CCM)
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
OBSERVATIONAL
Enrollment
120
Start Date
2025-07-10
Completion Date
2028-12-31
Last Updated
2025-07-29
Healthy Volunteers
No
Conditions
Interventions
Cardiac Contractility Modulation (CCM) implant
Subjects participating in the study carry or will carry the Cardiac Contractility Modulation (CCM) medical device "OPTIMIZER Smart Mini" by Impulse Dynamics (USA). It is indicated for use in patients over 18 years of age with symptomatic heart failure due to systolic left ventricular dysfunction, despite appropriate medical treatment. The OPTIMIZER Smart Mini Implantable Pulse Generator is a programmable device with an internal battery and telemetry functions. The OPTIMIZER Smart Mini is connected to two or three implantable leads, two of which are implanted in the right ventricle and one, optionally, in the right atrium.
Locations (13)
PO Anastasia Guerriero, Marcianise (CE), UOC Cardiologia
Marcianise, Campania, Italy
Clinica Montevergine, Mercogliano (AV), Laboratorio di Elettrofisiologia
Mercogliano, Campania, Italy
UOC Cardiologia, Osp. San Rocco, Sessa Aurunca (CE), ASL Caserta
Sessa Aurunca, Campania, Italy
Policlinico S.Orsola, UO Cardiologia
Bologna, Emilia-Romagna, Italy
OSPEDALE CASTELLI, UO Cardiologia
Anzio, Lazio, Italy
Elettrofisiologia e Aritmologia, ASST FBF Sacco
Milan, Lombardy, Italy
Fondazione Giglio, Cefalù (PA), UOC Cardiologia
Cefalù, Sicily, Italy
Osp. Generale Provinciale Mazzoni, UO Cardiologia
Ascoli Piceno, The Marches, Italy
UOC Cardiologia, Osp. Di Mirano, ULSS 3 Serenissima
Mirano, Veneto, Italy
UOC Cardiologia, Osp. Di Piove di Sacco (PD), ULSS 6 Euganea
Piove di Sacco, Veneto, Italy
UOC Cardiologia, Osp. S.Bortolo, Vicenza, ULSS 8 Berica
Vicenza, Veneto, Italy
UOC Cardiologia con UTIC, Osp. Di Venere
Bari, Italy
UO Cardiologia, S. Maria della Misericordia Hospital, ULSS5 Polesana
Rovigo, Italy