Methodology study on healthy participants
Conditions
Interventions
Group 1: Carrying out a non-contrast MRI examination of the lumbar spine, ankle, foot, knee, pelvis, and/or shoulder using the conventional (manual) workflow.
Immediately after completing each of the
Sponsors
Universitätsmedizin Göttingen
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Eligible participants are adult, healthy volunteers who are capable of providing informed consent and express interest in participating in the study.
Exclusion criteria
Exclusion criteria: Exclusion criteria include pre-existing conditions affecting the examined body regions, general contraindications to MRI examinations (i.e., claustrophobia, non-MRI-compatible implants, recent tattoos, pregnancy), or body dimensions that are not compatible with the scanner specifications.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Total examination time per subject (min:sec), time interval from the first MRI sequence to completion of the last diagnostic sequence, extracted from the DICOM metadata. | — |
Secondary
| Measure | Time frame |
|---|---|
| Number of necessary re-scans per examination. Source: protocol logs and technician documentation. Share of examinations with at least one re-scan (%). Source: protocol logs and technician documentation. Share of examinations with intervention from technicians (%). Source: Technician documentation. Time from completed patient positioning to completed examination ("table top time"), manually recorded by the MRI staff. | — |
Countries
Germany
Contacts
Public ContactSimon Friedrich Rösel
Universitätsmedizin Göttingen
Outcome results
None listed