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Prospective observational study on the clinical relevance of the combined PET / MR examination in pediatric oncology

Prospective observational study on the clinical relevance of the combined PET / MR examination in pediatric oncology - GK-PET/MR Tü-013

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00024123
Enrollment
55
Registered
2021-01-19
Start date
2014-07-30
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

C00-C97

Interventions

Group 1: Carry out at least two PET/MRI examinations: 1x basic examination before the start of therapy + 1x in the follow-up for therapy monitoring.

Sponsors

Universitätsklinikum Tübingen
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Months to 17 Years

Inclusion criteria

Inclusion criteria: Children or adolescents <18 years of age for whom the PET/MRI examination is carried out for the following indications: • PET/MRI examination for clinical indication for tumor search (e.g. FUO) • PET/MRI examination for clinical indication for primary staging or re-staging in Hodgin's lymphoma • PET/MRI examination for clinical indication for primary staging or re-staging after therapy in histologically proven, advanced malignant solid tumors (e.g. bone and soft tissue tumors, CNS tumors, neuroblastomas, germ cell tumors) • PET/MRI examination in the case of unclear or inconspicuous imaging for therapy planning (OP, RT, Ctx) and prognosis stratification • PET/MRI examination for re-staging in neurofibromatosis type I with the question of a malignant transformation of the neurofibromas and for biopsy or surgery planning • Written consent of the legal guardian and, if applicable, the child (depending on the individual stage of development) to participate in the study and to report so-called incidental findings after detailed explanation

Exclusion criteria

Exclusion criteria: • Presence of non-MRI-compatible implants or any kind of metal in and on the body (e.g. pacemakers, artificial heart valves, metal prostheses, implanted, magnetic metal parts, coils, etc.) • Children and adolescents who report a hearing disorder or an increased sensitivity to loud noises • Children and adolescents with reduced temperature sensation and/or increased sensitivity to warming of the body • pregnancy • Diabetes mellitus that cannot be controlled with medication

Design outcomes

Primary

MeasureTime frame
The study is primarily used for quality assurance and optimization of PET/MRI examinations in pediatric oncology. For PET/fMRI hybrid imaging, the clinical benefit for children and adolescents with solid tumors is to be determined. The clinical benefit is defined here as a change in patient management (diagnostic and therapeutic) based on the PET/MRI examination.

Secondary

MeasureTime frame
The data should be used to optimize the PET/MRI examination protocols with regard to possible time and dose reductions.

Countries

Germany

Contacts

Public ContactJürgen Schäfer

Radiologische Universitätsklinik Tübingen Diagnostische & Interventionelle Radiologie, Kinderradiologie

juergen.schaefer@med.uni-tuebingen.de07071-29-81489

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: May 1, 2026