Research and Development of Novel Quantitative Magnetic Resonance Imaging (MRI) Techniques in a Single Scan for Multiple Organ Application

ConditionMultiple
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorPerspectum

About this trial

Cross-sectional observational study to improve MRI data acquisition techniques by optimising MRI sequences for multiple organs and assessing the repeatability and reproducibility of multiparametric MRI, in healthy volunteers.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Adults aged 18 years and older

Participant is willing and able to give informed consent for participation in the study

The participant has a level of English proficiency that allows them to communicate well with the investigator and could comply with study requirements.

The participant is willing and able to undergo MRI scan.

Disqualifiers

Any contraindication to magnetic resonance imaging (incl. pregnancy, nonremovable electronic implants including cochlear implants, infusion pumps, and pacemakers, shrapnel injury, severe claustrophobia, allergic reaction to contrast agents)

Any other cause, including a significant disease or disorder which, in the opinion of the investigator, may either put the participant at risk because of participation in the study, or may influence the participant's ability to participate in the study

The participant may be excluded where body habitus is likely to make MRI or echocardiography/ultrasound uncomfortable or unlikely to yield analysable images, and BMI more than 40-45

Trial population

Study participants will be adult volunteers aged 18 and over, without a contraindication to magnetic resonance imaging.

Trial design

Design model

Other

Time perspective

Cross-sectional

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Development of MRI sequences

Development of sequences which will be used to collect good quality data on multiple organs across different MRI scanners and to ensure that desirable images are obtained within reasonable amount of time.

Time frame
7 years from study start

Secondary outcomes

1

Sequence and parameter validation

Validation of a list of sequences and parameter details

Time frame
7 years from study start
2

Assessment of MRI metric repeatability

Assessment of repeatability of the MRI metrics across 2 separate MRI acquisitions on the same scanner using statistical methods

Time frame
7 years from study start
3

Assessment of MRI metric reproducibility

Assessment of reproducibility of the MRI metrics in the same participants scanned on separate MRI scanners

Time frame
7 years from study start
4

Assessment of participant comfort during scan

Assessment of participant comfort during different MRI protocols with participant questionnaires.

Time frame
7 years from study start

Other outcomes

Sponsors and contacts

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