Healthy volunteers and patients are examined. A wide variety of diseases / health problems are examined in patients. The most important criterion is a clinically indicated MRI examination.
Conditions
Interventions
Group 1: In healthy subjects: Evaluation of MRI sequences and sequence order with regard to parameterization of the sequences, image quality and potential clinical application.
Group 2: For patients:
Sponsors
Universitätsklinikum Tübingen
Eligibility
Sex/Gender
All
Age
18 Years to 85 Years
Inclusion criteria
Inclusion criteria: Healthy subjects: - Healthy adults (male or female), - Age: 18-60 years, - Letter of acceptance (informed consent). Patients: - male and female patients, - Age: 18-85 years, - Letter of acceptance (informed consent), - Carrying out a clinically indicated MRI examination as part of clinical routine (no study-related intervention).
Exclusion criteria
Exclusion criteria: Healthy subjects: - MRI contraindications, - pregnancy / lactation, - claustrophobia, - Lack of consent to the communication of incidental findings. Patients: - MRI contraindications, - pregnancy / lactation, - Claustrophobia.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The aim of this research project is the evaluation of new, accelerated and robust MR-technologies with regard to their technical maturity and their information content. For this purpose, various MRI-techniques are to be used first on healthy volunteers and then on patients. | — |
Secondary
| Measure | Time frame |
|---|---|
| Quality assurance, reduction of MRI measurement times | — |
Countries
Germany
Contacts
Public ContactJudith Herrmann
Universitätsklinikum Tübingen, Radiologische Klinik, Abt. für Diagnostische & Interventionelle Radiologie
Outcome results
None listed