I25.0 I50.9
Conditions
Interventions
Group 1: Patients with a clinical indication for a cardiac MRI will receive, in addition to the clinically indicated (ECG-triggered) scans, additional scans triggered using a finger clip and VitalEye
Sponsors
Kardiale Bildgebung, Deutsches Herzzentrum der Charité
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Adult subjects/patients of any gender For patients: Scheduled, clinically indicated cardiac MRI examination The subject/patient is capable of understanding the procedures performed as part of the study and of giving informed consent Existing health insurance to ensure that any incidental findings can be further investigated
Exclusion criteria
Exclusion criteria: Minor subjects/patients Pregnancy Subjects/patients who are unable to understand the procedures performed as part of the study or to provide informed consent Claustrophobia General MRI contraindications For subjects: Known heart disease or more than mild pulmonary, hepatic, or renal disease
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Percentage of correctly identified heart beats via PPG in patients and volunteers | — |
Secondary
| Measure | Time frame |
|---|---|
| Percentage of correctly identified heart beats via PPG in patients with arrhythmia Image Quality and scan duration of scans triggered via PPG | — |
Countries
Germany
Contacts
Public ContactSebastian Kelle
Kardiale Bildgebung, Deutsches Herzzentrum der Charité
Outcome results
None listed