Evaluation of Cardiac Function With Cardio-respiratory Synchronized MRI
Study Details
Study Description
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.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Active Comparator: Normal Cardiovascular System 70 with a history of heart or lung disease |
Procedure: cardiovascular MRI (CMR)
CMR is used to demonstrate cardiac abnormalities and assess cardiac function in many patients
|
| Active Comparator: Abnormal Cardiovascular System 30 without any history of heart or lung disease |
Procedure: Conventional Cardiologic Evaluation
ECG (gating), and respiratory motion effects
|
Outcome Measures
Primary Outcome Measures
- Image Quality measured by resolution [10 Minutes]
- Image Quality measured by signal to noise [10 Minutes]
- Suitability for routine use measured by imaging time and ease of use [10 Minutes]
Eligibility Criteria
Criteria
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:
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electrical implants such as cardiac pacemakers or perfusion pumps
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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
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ferromagnetic objects such as jewelry or metal clips in clothing
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pre-existing medical conditions including a likelihood of developing seizures or claustrophobic reactions, and any greater than normal potential for cardiac arrest.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | New York University School of Medicine | New York | New York | United States | 10016 |
Sponsors and Collaborators
- NYU Langone Health
Investigators
- Principal Investigator: Leon Axel, New York University Medical School
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 14-00601