Actively Recruiting

Phase Not Applicable
Age: 20Years - 80Years
All Genders
Healthy Volunteers
NCT03854071

Development of Novel Physiological CMR Methods in Health and Disease

Led by Sheffield Teaching Hospitals NHS Foundation Trust · Updated on 2026-03-18

135

Participants Needed

1

Research Sites

648 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Physiological cardiovascular stress test plays a crucial role in the assessment of patients with suspected heart disease. There are several methods of cardiac physiological stress tests and each of them offer varied insight into cardiac physiological adaptation: passive leg raise, intra-venous fluid challenge, pharmacological stressors and physical exercise stress test. Echocardiography, which is the mainstay for the non-invasive rest/stress assessment of the left ventricular (LV) haemodynamics has several limitations. Novel methods of CMR imaging allow to map intra-cardiac flow in three-dimension using novel flow acquisitions. These novel flow acquisitions are called four-dimensional flow CMR, where the fourth dimension is time. Additionally, traditional cine CMR imaging for functional assessment can now be done without breath-holds using advanced acceleration methods, allowing them to be used during exercise. A comprehensive understanding of functional-flow coupling at rest, during increased pre-load (fluid challenge) to the heart or during exercise, is lacking in the literature. There is an important need to validate these novel CMR methods for developing mechanistic insight into physiological cardiac adaptation to increased pre-load or to exercise in health and how it alters in heart disease.

CONDITIONS

Official Title

Development of Novel Physiological CMR Methods in Health and Disease

Who Can Participate

Age: 20Years - 80Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Healthy volunteers aged 20 to 80, recruited from Sheffield Teaching Hospitals staff
  • Patients aged 20 to 80 with suspected or known heart disease in specified clinical groups
  • Ability to provide written informed consent
Not Eligible

You will not qualify if you...

  • Inability to complete the study protocol due to severe heart failure requiring intravenous therapy
  • History of myocardial infarction, acute coronary syndrome, or cardiomyopathy in suspected CAD and acute myocardial infarction groups
  • Significant valvular heart disease
  • Presence of atrial fibrillation
  • Contraindications to MRI as per standard screening

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Sheffield Teaching Hospitals NHS FT

Sheffield, England, United Kingdom, S10 2JF

Actively Recruiting

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Research Team

H

Helen Denney

CONTACT

A

Amber Ford

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

6

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