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Cardiac Magnetic Resonance Imaging After Cardiac Resynchronization Therapy

Cardiac Magnetic Resonance Imaging After Cardiac Resynchronization Therapy

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03183011
Enrollment
40
Registered
2017-06-09
Start date
2016-11-01
Completion date
2018-12-31
Last updated
2017-06-12

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

Conditions

Heart Failure, Systolic

Keywords

cardiac resynchronization therapy, implantable cardioverter defibrillator, heart failure, magnetic resonance imaging

Brief summary

This study is evaluating how MRI after CRT can provide key insights regarding LV function, structure, and mechanics resulting from CRT in patients with or without LV scar and inform optimal pacing strategies. The expected accurate and reproducible response assessment with cardiac MRI has important implications for evaluating CRT outcomes in clinical trials, and the insights from the post-CRT MRI promise to improve implementation of CRT.

Detailed description

We are performing a study of 40 patients with current accepted indications for CRT and no MRI contraindications. These patients will have a pre-CRT MRI and another post-CRT MRI 6 months after the CRT procedure. Echocardiography, cardiopulmonary exercise testing, symptom assessment, and laboratory testing are also performed before and after CRT. Modifications to the post-CRT MRI protocol include the use of gradient echo cine imaging rather than steady state free precession imaging, application of wideband imaging to the LGE acquisitions, and strain imaging with cine Displacement Encoding with Stimulated Echoes (DENSE) tailored for device patients.

Interventions

OTHERMRI

Cardiac MRI

Sponsors

Kenneth Bilchick, MD
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
25 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Chronic systolic HF * LVEF 35% or less * Guideline-based class I or IIa indication for CRT * 25 and 85 years old * Predominantly in sinus rhythm * GFR ≥ 40 ml/min/1.73m2\* \*Contrast will not be given for the 6-month follow-up scan if the GFR falls to \< 40 ml/min/1.73m2.

Exclusion criteria

* Inability to provide informed consent * Pregnancy * Presence of metal embedded in the body due to prior accident or injury, as documented by skull films or other imaging * Preexisting pacemaker or defibrillator prior to enrollment * Cerebral aneurysm clips; 6) cochlear implants * Other metallic implants (prior to enrollment) known to be contraindications to MRI * Severe claustrophobia * Acute kidney injury * Acute renal failure or chronic kidney disease with GFR \< 40 cc/min * Liver transplant * Gadolinium allergy

Design outcomes

Primary

MeasureTime frameDescription
CRT Response1 yearCRT Response

Countries

United States

Contacts

Primary ContactKenneth C Bilchick, MD
bilchick@virginia.edu434-924-2465

Outcome results

None listed

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