Skip to content

MRI Sequence and Imaging Protocol Development

MRI Sequence and Imaging Protocol Development

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03040947
Acronym
BikeMRI
Enrollment
200
Registered
2017-02-02
Start date
2016-03-31
Completion date
2022-12-31
Last updated
2021-03-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiomyopathy, Hypertrophic, Cardiomyopathy, Dilated, Left Ventricular Hypertrophy, Ischemic Heart Disease, Hypertension

Brief summary

The purpose of this study is to develop imaging protocols when using cardiovascular magnetic resonance (CMR) to assess cardiac functions, morphology and tissue characterization. The National Heart Research Institute Singapore (NHRIS) houses two dedicated CMR scanners to support the numerous investigator initiated projects in patients with various cardiac pathologists. By optimizing novel CMR sequences used in these studies, scanning time can be shortened for patients with underlying cardiac diseases.

Detailed description

In medical research, there is a continuous need to develop new imaging techniques such as cardiovascular magnetic resonance (CMR) imaging. This will allow us to visualize and study the function and structure of the heart in greater detail so as to improve the diagnosis and treatment of patients with various cardiac conditions. The aim of the study is to optimise new CMR sequences, allowing the development of imaging protocols in future research studies. This study will hence recruit 800 subjects for each of the following sub-studies: 1. Sub-study 1: Normal CMR protocols for assessment of cardiac function and morphology 2. Sub-study 2: Exercise stress protocols with a CMR-compatible supine bike. For the first sub-study, 400 healthy volunteers and patients with cardiac conditions or suspected to have cardiac conditions will be recruited. The testing and optimising of CMR sequence settings are crucial to ensure the accuracy and robustness of the scan before using the scan as a clinical diagnostic tool. For the second sub-study, 400 healthy volunteers of different fitness levels and and patients with cardiac conditions or suspected to have cardiac conditions will be recruited. An exercise stress protocol will then be developed for future studies in patients with suspected coronary artery diseases. For this protocol, participants will be asked to cycle on a supine exercise bike to assess the effects of exercise and free breathing on the stability of the CMR imaging sequences.

Interventions

Sponsors

National Heart Centre Singapore
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
21 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* Has no known significant medical history * Is able to give informed consent

Exclusion criteria

* Has contraindications to CMR implantable devices, cerebral aneutysm clips and cochlear implants * Has claustrophobia * Females who are pregnant * Is unable to comply with study protocols

Design outcomes

Primary

MeasureTime frameDescription
First occurrence of cardiovascular event1 dayThis outcomes are obtained via hospital records or by a phone follow-up

Countries

Singapore

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026