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Clinical applications of GESE-EPIK sequences in MRI (GESE-EPIK), a prospective, monocentric, other study to evaluate the cerebral oxygen extraction fraction

Clinical applications of GESE-EPIK sequences in MRI (GESE-EPIK), a prospective, monocentric, other study to evaluate the cerebral oxygen extraction fraction - GESE-EPIK-MRT

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00032647
Enrollment
400
Registered
2024-02-02
Start date
2024-06-01
Completion date
Unknown
Last updated
2026-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tumors, vascular diseases, neurodegenerative diseases

Interventions

Group 1: Magnetic resonance imaging (MRI) examinations that are performed as part of the clinical routine and are clinically indicated are supplemented by an additional modified standard sequence ("GE

Sponsors

Uniklinikum RWTH Aachen
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: The patients are examined as part of a clinically indicated MRI examination (clinical routine). In principle, all patients with the above-mentioned clinical pictures who are suitable for MRI examinations can be included. MRI examination to clarify a disease from the following types: • Vascular diseases (e.g. stenosis of the arteries supplying the brain) • Tumor diseases (e.g. brain tumors) • Neurodegenerative diseases (e.g. Alzheimer's disease) • Inflammatory, metabolic or immunological diseases (e.g. multiple sclerosis) • Malformations (e.g. schizencephaly) • Trauma (e.g. condition after traumatic brain injury)

Exclusion criteria

Exclusion criteria: Patients under the age of 18 are excluded. Patients who cannot undergo a routine MRI examination due to contraindications cannot participate in the study. These are patients who carry certain electrical devices (e.g. pacemakers, drug pumps, etc.) or certain metal parts (e.g. screws after bone fractures) in or on the body and/or patients who suffer from claustrophobia. Pregnancy (exclusion by means of a urine test) Patients whose examination would require additional time, which could delay any necessary acute therapy, are also excluded from participation in the study. Patients for whom prolonged lying in the scanner is a burden (e.g. due to back problems or restlessness). Patients who are deprived of their liberty on the basis of an official or court order or authorization.

Design outcomes

Primary

MeasureTime frame
The aim of the research project is to compare OEF values in the various pathologies with healthy values in order to characterize possible dependencies and changes. The healthy contralateral hemisphere can serve as an intraindividual comparison. The comparison to healthy individuals can (subsequently) also be made using among others values from the literature.

Countries

Germany

Contacts

Public ContactDimah Hasan

Uniklinik RWTH Aachen

dhasan@ukaachen.de+492418089602

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Apr 4, 2026