Healthy volunteers without any known cardiac disease Not Applicable
Conditions
Interventions
After enrolment participants will be scanned on both clinical as well as the ultra-high-field scanners.
Scan protocol involves one hour of scan time each, during which the ECG-electrod
Sponsors
Charité University Medicine Berlin
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. > 18 years 2. Written consent
Exclusion criteria
Exclusion criteria: 1. Any known cardiac disease 2. Contraindication to CMR
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Gating quality assessed by calculating jitter (in ms), performance index and propagation delay (in ms) from evaluating the recorded trigger timepoints against the manually annotated recorded ECG-trace. The annotation will be performed by two independent observers. | — |
Secondary
| Measure | Time frame |
|---|---|
| Image quality assessed semiquantitatively by two observers by using a visual rating scale | — |
Countries
Germany
Outcome results
None listed