Ion Therapy Patient Registry

  • End date
    Dec 8, 2032
  • participants needed
  • sponsor
    EBG MedAustron GmbH
Updated on 8 March 2021


The purpose of the study is the prospective and standardized data collection of patients treated with ion therapy at MedAustron.


During and up to 10 years after radiation therapy data regarding tumor control and treatment response as well as acute and late toxicities will be collected at regular time intervals. Additionally quality of life and sociodemographic status will be assessed in all study patients and neurocognitive assessment will be performed in patients undergoing ion radiation of the brain.

Condition Ion Beam Radiation Therapy for Tumor Patients
Treatment Protons and Carbon Ions
Clinical Study IdentifierNCT03049072
SponsorEBG MedAustron GmbH
Last Modified on8 March 2021


Yes No Not Sure

Inclusion Criteria

Patients with tumor disease treated with ion beam therapy at MedAustron
Signed informed consent form

Exclusion Criteria

Comorbidities endangering treatment delivery or study compliance
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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