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Dynamic EchoCardiographic Optimisation REsponse Study (DECORE)

I

Institute of Hospitalization and Scientific Care (IRCCS)

Status

Enrolling

Conditions

Heart Failure

Study type

Observational

Funder types

Other

Identifiers

NCT05473481
2752/6065

Details and patient eligibility

About

The aim of this study is to evaluate the effects of heart rate optimization and guided A-V and V-V delay from color Doppler echocardiography, in subjects affected by heart failure with reduced ejection fraction and CRT-D device wearers who did not respond to device implantation in clinical, electrophysiological, and other terms.

Enrollment

73 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patient must be 18 to 85 years of age inclusive, at the time of signing the informed consent form;
  2. Heart failure with ventricular ejection fraction left <45%;
  3. Presence of CRT-D devices in a non-responder patient for cardiac resynchronization
  4. NYHA >II;
  5. Resting heart rate <65 beats per minute;
  6. Biventricular pacing >97%.

Exclusion criteria

  1. Age <18 and >85 years;
  2. Insufficient functional capacity to complete the tests required by the research protocol;
  3. Permanent Atrial Fibrillation

Trial contacts and locations

1

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Central trial contact

Massimo Saviano, MD

Data sourced from clinicaltrials.gov

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