HyperArc Registry VAR-2019-01
HyperArc Registry Study
Trial summary:
The HyperArc registry is designed to collect data from which the efficacy of the HyperArc procedure can be assessed and compared to alternative treatments.
Receptor status / problem studied:
Inclusion criteria
- Received or scheduled to receive treatment using the HyperArc treatment method
- Age of legal adult according to local law
- Signed informed consent form, or, informed consent waived by the local ethics board/institutional review board
Exclusion criteria
- None, apart from not meeting Inclusion Criteria
Open for recruitment
Trial Title
HyperArc Registry VAR-2019-01
Diagnosis
Brain cancer
Type of trial
Pharmaceutical
Type of treatement
Radiation Oncology Radiation Medicine
Phase
Registry
Locations
Investigators
Principal Investigator