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Evaluation of Cardiac Function With Cardio-respiratory Synchronized MRI

Evaluation of Cardiac Function With Cardio-respiratory Synchronized MRI

Status
Suspended
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02728284
Enrollment
100
Registered
2016-04-05
Start date
2018-03-29
Completion date
2027-08-31
Last updated
2026-01-05

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

Conditions

Heart Disease

Keywords

Magnetic Resonance Imaging (MRI)

Brief summary

The purpose of this investigation is to evaluate newer methods of performing cardiovascular MRI (CMR) that will provide new kinds of information related to the interplay between the cardiac and the respiratory cycles, such as the interaction between the left ventricle and the right ventricle during respiration . The primary statistical objective is to provide preliminary indications of the relative utility of the investigational imaging software in terms of image quality and suitability for routine clinical use. Image quality will be expressed in terms of signal-to-noise ratios (SNR), contrast-to-noise ratios (CNR) and subjective Likert-type qualitative assessments independently provided by each of multiple blinded readers for each image. Suitability for routine use will be assessed in terms of imaging time and a binary indicator of whether, in the opinion of the investigator, adverse procedural complications (not expected) were encountered during a given imaging session.

Interventions

PROCEDUREcardiovascular MRI (CMR)

CMR is used to demonstrate cardiac abnormalities and assess cardiac function in many patients

PROCEDUREConventional Cardiologic Evaluation

ECG (gating), and respiratory motion effects

Sponsors

NYU Langone Health
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
7 Years to 95 Years
Healthy volunteers
No

Inclusion criteria

* Subjects will be selected as they are scheduled for clinical MR examinations. * Subjects will be selected on the basis of their willingness and ability to participate, on their comprehension of the informed consent document, on their likelihood of completing the study, and on the clinical appropriateness of the investigational technique for a given patient.

Exclusion criteria

* electrical implants such as cardiac pacemakers or perfusion pumps * ferromagnetic implants such as aneurysm clips, surgical clips, prostheses, artificial hearts, valves with steel parts, metal fragments, shrapnel, tattoos near the eye, or steel implants * ferromagnetic objects such as jewelry or metal clips in clothing * pre-existing medical conditions including a likelihood of developing seizures or claustrophobic reactions, and any greater than normal potential for cardiac arrest.

Design outcomes

Primary

MeasureTime frame
Image Quality measured by resolution10 Minutes
Image Quality measured by signal to noise10 Minutes
Suitability for routine use measured by imaging time and ease of use10 Minutes

Countries

United States

Outcome results

None listed

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