Skip to content

Revisit the Value of Imaging in Best Using CArdiac Resynchronization Therapy

Revisit the Value of Imaging in Best Using CArdiac Resynchronization Therapy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02528032
Acronym
RICART
Enrollment
80
Registered
2015-08-19
Start date
2015-08-31
Completion date
2018-09-30
Last updated
2023-05-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Resynchronization Therapy

Keywords

Left ventricular dysfunction, Other cardiac dysrhythmias

Brief summary

Many studies have shown the benefits of cardiac resynchronization therapy (CRT) with biventricular pacing in patients with heart failure with left ventricular dysfunction. CRT restores contraction coordination between different regions of the left ventricle, which yields a significant improvement in LV systolic function, symptoms, exercise tolerance and quality of life. In the longer term, treatment with resynchronization induces a reverse remodeling of the left ventricle and a decrease in mortality and morbidity (hospitalization for heart failure). Nevertheless, even if a majority of patients treated with CRT feel the benefit, some (up to 40% depending on the response criteria of CRT) do not experience significant improvement (nonresponders). Echocardiography and imaging have not so far demonstrated their added value to optimize delivery of CRT. Monocentric promising work on limited numbers of patients, however, were carried out. Meanwhile, equipment for delivering CRT evolves and new probes with four poles stimulation of the left ventricle are now used. The objective of this research is to validate new sequences of ultrasound processing estimating the CRT. These tools are based on usual echocardiographic examination of patients

Detailed description

Pilot study for testing tools pre and post-treatment images echocardiography but also MRI with a descriptive purpose and identification of the computed parameters should be secondarily test a large multicenter cohort . Patients in the study will be explored in RICART preimplantation as then in the manner used in current clinical routine. The use of data by cons will focus on the study of new tools ever compared in the same patients. Data echocardiography (as with other techniques) are those used in clinical routine. Then, the data processing to be carried characterized the asynchrony posteriori, regardless of initial clinical data on a dedicated search software. Each quantitative parameter will be compared with others in order to predict the response to resynchronization. Response prediction of threshold values to the resynchronization can be obtained and compared to each of the tools. The value of relative and an addition to another may be tested. The predictive value of the change (delta) of each parameter between the pre- and post-implantation to predict response to al resynchronization, will be evaluated.

Interventions

OTHEREchographic evaluation of heart function

Echocardiographic data collection and analysis, not fully exploited at present

Sponsors

Rennes University Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Any patient with sinus rhythm sent to hospital for a cardiac resynchronization according to ESC criteria and implanted with a left ventricular pacing lead quadrupole

Exclusion criteria

* Patients with an acoustic window is incompatible with the accurate echographic assessment of heart function * Patients with spontaneous one year prognosis is not dependent on his heart or another disease to the forefront (eg neoplasia) * Contra-indications to MRI (pacemaker or implantable defibrillator, intracranial ferromagnetic surgical clips, cochlear implants, intraocular metallic foreign body, Starr-Edwards heart valve prosthesis pre 6000, biomedical device type pump insulin or neurostimulator) or against -indications to iodinated contrast injection (severe renal impairment, allergy). * Patient not giving free and informed consent.

Design outcomes

Primary

MeasureTime frameDescription
Measuring the prognostic value of a package of new ultrasonic signal processing toolspre-implantationTo evaluate the prognostic value of a package of new tools quantitatively measuring mechanical dyssynchrony prior to implantation of a resynchronization pacemaker in terms of favorable response at 6 months.

Secondary

MeasureTime frameDescription
Compare pre and post-implantation asynchrony characterisationpre-implantation, and within three day post implantationpre and within three day post implantation mechanical asynchrony by package of new tools will be compared with the same characterization of biventricular pacemaker.
Characterization of the pre-implantation mechanical asynchrony by package of new toolspre-implantationThe characterization of the pre-implantation mechanical asynchrony with the package of tested tools will be correlated with the results of: * Replacement fibrosis mark (taking gadolinium) and interstitial fibrosis (T1 mapping) \[MRI\] * Evaluation of the coronary venous system by chest CT
Analysis and comparison of cardiac mechanical asynchrony characterization tools with other asynchronism criteria already describeat 6 monthcardiac mechanical asynchrony characterization tools will be analyzed and compared, associated with other asynchronism criteria already described defined by the reverse LV remodeling 6 months post-implantation (positive response regressions = ≥15% of tele-systolic volumes VG 6 months) to define the best or the best combination of predictive tools of the response to the CRT)
Prediction scoreat 6 monthdefinition of a prediction score of the answer to the CRT (echocardiographic and multi-modality)

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026