NCT06012890

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.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
150

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Aug 2023

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 1, 2023

Completed
13 days until next milestone

First Submitted

Initial submission to the registry

August 14, 2023

Completed
14 days until next milestone

First Posted

Study publicly available on registry

August 28, 2023

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 31, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 31, 2024

Completed
Last Updated

August 28, 2023

Status Verified

August 1, 2023

Enrollment Period

1 year

First QC Date

August 14, 2023

Last Update Submit

August 21, 2023

Conditions

WorkflowTime

Outcome Measures

Primary Outcomes (1)

  • Overall scan time

    This study's primary endpoint will be the overall scan time, from first to last MRI image acquired.

    Up to 12 months

Study Arms (2)

Automatic acquisition

Clinical MRI planning performed automatically by an AI-based software

Other: Automation of cardiac MRI acquisition

Manual Acquisition

Clinical MRI planning performed manually by a specialized radiology technician

Interventions

Automation of cardiac MRI acquisitionOTHER

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

Automatic acquisition

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

General population referred for morphological cardiac MRI, with consecutive patient sampling.

You may qualify if:

  • 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.

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University Hospital, Geneva

Geneva, Switzerland

RECRUITING

Study Officials

  • Carl Glessgen, MD

    Radiologist

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Carl Glessgen, MD

CONTACT

00795536227carl.glessgen@hcuge.ch

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Medical Doctor, Consultant

Study Record Dates

First Submitted

August 14, 2023

First Posted

August 28, 2023

Study Start

August 1, 2023

Primary Completion

July 31, 2024

Study Completion

July 31, 2024

Last Updated

August 28, 2023

Record last verified: 2023-08

Data Sharing

IPD Sharing
Will not share

Locations

CH(1)