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Performance of Acquisition Automation of Cardiac MRI

Impact of Acquisition Automation on the Duration and Quality of Cardiac MRI Examinations

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06012890
Enrollment
150
Registered
2023-08-28
Start date
2023-08-01
Completion date
2024-07-31
Last updated
2023-08-28

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

Conditions

Time, Workflow

Brief summary

For this study, cardiac MRI examinations performed will be prospectively included and realized either fully automatically or by a specialized radiology technician. The duration of the automated examinations will be compared to the duration of the manual examinations. The number of failed sequences in both study arms (automated and manual) will be recorded and the quality of the cardiac planes will be compared.

Detailed description

The main hypothesis is that fully automated cardiac MRI protocols require shorter overall scan times than manually acquired, human-executed protocols. The objective will be to demonstrate that automating the examination allows to shorten the scan time, leading to increased patient comfort and clinical flexibility. The study's secondary objective will be to demonstrate the non-inferiority of the automated protocol compared to human acquisition in terms of resulting planning quality and error occurrence during slice planning. Included patients will undergo clinical cMRI following international and national standards: only the acquisition strategy will vary. The investigators will successively recruit patients presenting for routine cardiac MRI. The acquisition strategy of the MRI - either automated or manual - will alternate to avoid comparison bias. The MRI protocol will be the same for both arms and consists of standardized sequences acquired before and after contrast administration. Recruitment will be performed at a single location, in the radiology department. Patients will be recruited on a daily, consecutive basis during clinical practice. No questionnaire will be used for this study. No biological material will be sampled. Observational data about the acquisition process, potential errors, and patient characteristics will be recorded.

Interventions

OTHERAutomation of cardiac MRI acquisition

The intervention will consist of the automation of the cMRI examination.

Sponsors

University Hospital, Geneva
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Adult patient presenting for morphologic and functional assessment of the myocardium by cardiac MRI. * Research consent form obtained after information procedure. * Complete cardiac MRI protocol performed.

Exclusion criteria

* Patients unable to provide informed consent. * Implantable cardiac device * Incomplete cardiac examination due to early termination by the patient. * Incomplete data on examination parameters (missing forms). * Incompatible MRI protocol

Design outcomes

Primary

MeasureTime frameDescription
Overall scan timeUp to 12 monthsThis study's primary endpoint will be the overall scan time, from first to last MRI image acquired.

Countries

Switzerland

Contacts

Primary ContactCarl Glessgen, MD
carl.glessgen@hcuge.ch00795536227

Outcome results

None listed

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