Optimization and evaluation of modern MRI techniques for acceleration and artifact reduction in pathologies of the skull base

Institut für Radiologie und Neuroradiologie Evangelisches Krankenhaus Oldenburg, Universitätsmedizin Oldenburg0 sites70 target enrollmentApril 8, 2022

Conditionsisted exemplary ICH codes in an openly designed study, which covers a broader spectrum of skull base lesions: H.90.0 - H.90.8, H.91.0, H91.9, H93.8, H93.9, D33.1, D33.3, D33.7, D33.9, D32.9, D36.1, C.72.5

Overview

Phase: Not Applicable
Intervention: Not specified
Conditions: isted exemplary ICH codes in an openly designed study, which covers a broader spectrum of skull base lesions: H.90.0 - H.90.8, H.91.0, H91.9, H93.8, H93.9, D33.1, D33.3, D33.7, D33.9, D32.9, D36.1, C.72.5
Sponsor: Institut für Radiologie und Neuroradiologie Evangelisches Krankenhaus Oldenburg, Universitätsmedizin Oldenburg
Enrollment: 70
Status: Not yet recruiting
Last Updated: last year

Overview Investigators Eligibility Criteria Outcomes Similar Trials

Overview

Brief Summary

No summary available.

Registry

who.int

Start Date

April 8, 2022

End Date

TBD

Last Updated

last year

Study Type

Observational

Sex

All

Investigators

Sponsor

Institut für Radiologie und Neuroradiologie Evangelisches Krankenhaus Oldenburg, Universitätsmedizin Oldenburg

Eligibility Criteria

Inclusion Criteria

•General: persons with a minimum age of 18 years who are able to give their informed consent
•Subproject 1 and 2, Step 1: Healthy Volunteers
•Subproject 1, Step 2: Patients for CI evaluation (screening MRI examination for the exclusion of abnormalities of the auditory nerves, inner ears and central auditory path)
•Subproject 2, Step 2: Patients with known or suspected untreated skull base lesions (e.g. vestibular Schwannomas, pseudotumors of the orbit, paragangliomas)

Exclusion Criteria

•\- General MRI contraindications for MRI, e.g. implants such as non\-conditional MR\-suitable pacemakers or auto\-defibrillators, implanted neural stimulators and ocular metal foreign bodies (e.g. metal shards)
•\- Conditions that could hinder the conduct of the study (e.B. morbid obesity, pronounced claustrophobia)
•\- Existing unnecessary risks (pregnancy, surgery of an unsafe nature).
•Subproject 1 and 2, Step 1: Known serious disease of the central nervous system.
•Subproject 1, Step 2: Known serious disease of the central nervous system (other than possibly the one associated with hearing loss in the patient group).
•Subproject 2, Step 2: Known serious disease of the central nervous system (except skull base lesions in the patient group)