Real-time MRI for Evaluating Cardiac Volumetry

Last updated: November 24, 2023
Sponsor: University of Leicester
Overall Status: Active - Recruiting

Phase

N/A

Condition

Birth Defects

Holoprosencephaly

Treatment

cardiovascular magnetic resonance

Clinical Study ID

NCT05221853
0768
270285
  • Ages > 18
  • All Genders

Study Summary

This study will compare the accuracy of a real-time Cine sequence in assessing cardiac volumetry.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Patients aged ≥ 18 years
  2. Referred for routine CMR imaging
  3. Willing and able to give informed consent
  4. Willing and able to comply with the requirements of the study
  5. Able to understand written English

Exclusion

Exclusion Criteria:

  1. Severe claustrophobia
  2. Absolute contraindications to CMR (those with CMR conditional or safe devices will beeligible for inclusion)
  3. Unable to provide informed consent
  4. Participants unable to understand written English

Study Design

Total Participants: 570
Treatment Group(s): 1
Primary Treatment: cardiovascular magnetic resonance
Phase:
Study Start date:
February 23, 2021
Estimated Completion Date:
February 01, 2025

Study Description

This is a single-centre prospective study involving up to 570 patients with known or suspected cardiac disease referred for routine clinical cardiovascular magnetic resonance (CMR) assessment at Glenfield General Hospital, Leicester. In addition to standard multi-breath-hold steady-state free precession (SSFP) imaging (undertaken as part of the routine scan), each patient will also undergo additional imaging with a non-breath-hold multi-slice real-time cine sequence.

The primary outcome is the assessment of cardiac volumetry and function (end-diastolic volume, end-systolic volume, stroke volume, ejection fraction and myocardial mass) as measured by (1) the standard multi-breath-hold SSFP technique and (2) the non-breath-hold multi-slice real-time cine sequence. Secondary outcome measures will be (1) the time required for each scan, and (2) image quality for each scan. An additional secondary outcome will be to compare indexed cardiac volumes with those indexed according to measured body-surface area.

Connect with a study center

  • Glenfield Hospital

    Leicester, Leics LE3 9QP
    United Kingdom

    Active - Recruiting

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.