Actively Recruiting

Age: 18Years - 80Years
All Genders
Healthy Volunteers
ID01728597

Optimization of Non-contrast Enhanced 1.5 Tesla and 3 Tesla Cardiac Magnetic Resonance Imaging Techniques and Acquisition of Normal Values

Led by Medical University of Graz · Updated on 2025-02-12

200

Participants Needed

1

Research Sites

104 weeks

Total Duration

On this page

Sponsors

M

Medical University of Graz

Lead Sponsor

A

Amt der Steiermärkischen Landesregierung, Abteilung 3

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating and optimizing cardiac magnetic resonance (MR) imaging techniques at 1.5 Tesla and 3 Tesla strengths without the use of contrast agents. The study focuses on improving image quality and adapting protocols based on individual patient anatomy and physiology. It aims to establish normal values for new cardiac MR imaging methods, including myocardial morphology, cardiac function, anatomy, and blood flow measurements. The study involves MR-compliant volunteers without a history of cardiovascular diseases. Various imaging sequences are used to assess normal myocardial morphology through T1-, T2-, and T2*-weighted imaging, cardiac function including systolic and diastolic performance, coronary artery anatomy, and blood flow characteristics such as velocity, vorticity, and timing. Data acquisition and protocol optimization are conducted without applying contrast agents. Participants undergo detailed cardiac MR scans within one week, during which multiple parameters like cardiac volumes, muscle mass, coronary artery anatomy, and various blood flow metrics are measured. The collected data help define normal ranges for magnetic relaxation times and cardiac function. The study involves healthy volunteers aged 18 to 80 years and includes screening for MR compatibility and ability to consent. Safety measures exclude individuals with metal implants, pregnancy, or claustrophobia.

CONDITIONS

Brief Title

Non-contrast Enhanced Cardiac Magnetic Resonance Normal Values and Imaging Protocols

Who Can Participate

Age: 18Years - 80Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • No history of cardiac or pulmonary diseases
  • Ability to give informed consent
  • Age between 18 and 80 years
  • MR compliant volunteers with no contraindications for MRI
Not Eligible

You will not qualify if you...

  • Presence of metal devices or magnetic materials in or on the body that are hazardous for MRI (e.g., pacemaker, brain aneurysm clip, nerve stimulators, electrodes, penile implants, colored contact lenses, medication patches, metal implants like rods, joints, plates, pins, screws, nails, clips, embolization coils, or metal fragments/shrapnel)
  • Pregnancy
  • Claustrophobia

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Up to 1 week

Participants undergo non-contrast enhanced cardiac magnetic resonance imaging to acquire normal cardiac values and imaging data.

1 visit (in-person)

Trial Site Locations

Total: 1 location

1

Medical Unitersity Graz, Department of Radiology, Division of General Radiology

Graz, Styria, Austria, 8036

Actively Recruiting

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Research Team

U

Ursula Reiter, PhD

M

Michael Fuchsjäger, Prof. Dr.

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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Published Research Related To This Trial

Evaluation of left ventricular and left atrial volumetric function from native MR multislice 4D flow magnitude data.

Clemens Reiter, Gert Reiter, Corina Kräuter...

https://pubmed.ncbi.nlm.nih.gov/37580598