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Feasibility of Online MR-guided Radiotherapy on a 1.5T MR-Linac

Feasibility of Imaging and Radiotherapy on a Novel 1.5 T Hybrid Magnetic Resonance Imaging - Linear Accelerator System (MR-Linac)

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04172753
Enrollment
472
Registered
2019-11-21
Start date
2018-05-09
Completion date
2027-05-09
Last updated
2019-11-21

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

Conditions

Breast Cancer, Esophageal Cancer, Head and Neck Cancer, Liver Cancer, Oligometastasis, Prostate Cancer, Rectal Cancer

Keywords

Radiotherapy, Adaptive Radiotherapy

Brief summary

This study investigates the feasibility of imaging and treatment on a novel 1.5 T MR-Linac radiotherapy hybrid device.

Detailed description

Novel hybrid devices combine magnetic resonance imaging (MRI) and a linear accelerator in a single device. The superior soft tissue contrast compared with cone-beam computed tomography based treatment and the possibility for daily plan adaptation promise a higher precision of treatment, better target volume coverage and normal tissue sparing. In a first step the present study will test the feasibility of imaging and treatment on the 1.5 T MR-Linac.

Interventions

RADIATIONRadiotherapy on the MR-Linac

Radiotherapy is performed on the 1.5 T MR Linac

DIAGNOSTIC_TESTImaging on the MR Linac

Only imaging performed on the MR Linac

Sponsors

University Hospital Tuebingen
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* existing indication for radiation therapy * minimum age 18 years, no upper age limit * capacity for consent * Informed consent

Exclusion criteria

* contraindication for MRI (claustrophobia, metallic implants not applicable for MRI * pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Feasibility of online MR guided RadiotherapyDuring every single patients treatment (i.e. between one to seven weeks after the first application of radiotherapy)Treatment of a patient is considered feasible when 85% of treatments were completed as planned in this patient

Secondary

MeasureTime frameDescription
Time analysisDuring every single patients treatment (i.e. between one to seven weeks after the first application of radiotherapy)Time required for online MR guided radiotherapy

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026