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Clinical Trials/NCT04902079
NCT04902079
Unknown
Not Applicable

Observational and Prospective Registry on Cardiac Contractility Modulation (CCM) Therapy

Monaldi Hospital1 site in 1 country20 target enrollmentMarch 8, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Heart Failure, Systolic
Sponsor
Monaldi Hospital
Enrollment
20
Locations
1
Primary Endpoint
Improvement Quality of Life
Last Updated
4 years ago

Overview

Brief Summary

Observational and perspective study with acute and chronic endpoint.

Detailed Description

This registry includes patients who have undergone implantation of the cardiac contractility modulation device due to the presence of heart failure with reduced left ventricular systolic function and symptomatic despite optimal therapy, as indicated in the guidelines of the ESC of 2016 and the Expert Consensus Document of the ESC Heart Failure group published in May 2019 for to assess the benefits after the CCM device.

Registry
clinicaltrials.gov
Start Date
March 8, 2021
End Date
December 31, 2023
Last Updated
4 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Monaldi Hospital
Responsible Party
Principal Investigator
Principal Investigator

Antonio D'Onofrio

Head of UOSD Elettrofisiologia Studio e Terapia delle Aritmie

Monaldi Hospital

Eligibility Criteria

Inclusion Criteria

  • Male or non-pregnant female, aged 18 or older;
  • chronic heart failure with symptomatic left ventricular systolic function; (NYHA class II-IVa) with or without device already implanted (for example AICD, pace-maker);
  • Appropriate and optimized medical therapy
  • Patient signed and dated informed consent form at enrollment;
  • life expectancy\> 1 year due to the absence of comorbidities that reduce the prognosis

Exclusion Criteria

  • absence of venous access available for implant;
  • contraindication to the interventional procedure of CCM device implant (for example presence of Mechanical tricuspid vale);
  • pregnant patients

Outcomes

Primary Outcomes

Improvement Quality of Life

Time Frame: 12 months

Evaluatation of the impact on CCM Therapy on Quality of Life evaluated from the reduction of MLWHFQ score at FU post implant of CCM device compared to baseline

Functional Capacity

Time Frame: 12 months

Evaluation of the impact on CCM Therapy on Functional Capacity evaluated from the gain of distance traveled in the 6MWT at FU post implant of CCM device compared to baseline

Reduction of HF Hospitalizations and Emergency Ward accesses

Time Frame: 12 months

Reduction of HF Hospitalizations and Emergency Ward accesses at FU post implant of CCM device compared to number of HF hospitalization an Emergency Ward accesses collected 1 year before the implant of CCM therapy

Study Sites (1)

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