MedTrace Logo

Normal Reference Values for 3T Cardiac Parametric Mapping

NCT06784427 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 143

Last updated 2025-01-20

No results posted yet for this study

Summary

This is a study non-randomised and uncontrolled cross-sectional experimental/interventional study.

Consecutive subjects will be enrolled healthy, volunteer subjects to undergo a Cardio-RM examination on the new 3T MRI equipment.

The Cardio-RM examination to which they will undergo: does NOT involve the administration of contrast medium involves the performance of certain preliminary 'localisation' sequences.

Following the execution of the investigation the investigators will use the post-processing workstations to analyse the parametric sequences and extract the T1 and T2 values of the myocardium.

To minimise bias, two different investigators different experimenters independently evaluate the sequences, in order to assess inter-observer agreement; furthermore, to assess the stability of the acquisition of these sequences, temperature and humidity will be measured of the MRI room for each survey performed.

Conditions

  • Cardiac Imaging
  • Cardiac Imaging Techniques

Sponsors & Collaborators

  • IRCCS Azienda Ospedaliero-Universitaria di Bologna

    lead OTHER

Principal Investigators

  • Edoardo Rasciti, MD · IRCCS Azienda Ospedaliero-Universitaria di Bologna

Eligibility

Min Age
20 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-09-26
Primary Completion
2024-04-19
Completion
2024-04-19

Countries

  • Italy

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06784427 on ClinicalTrials.gov