RECRUITING

HyperArc Registry Study

Description

The HyperArc registry is designed to collect data from which the efficacy of the HyperArc procedure can be assessed and compared to alternative treatments.

Study Overview

Study Details

Study overview

The HyperArc registry is designed to collect data from which the efficacy of the HyperArc procedure can be assessed and compared to alternative treatments.

HyperArc Registry Study

HyperArc Registry Study

Condition
Brain Metastases
Intervention / Treatment

-

Contacts and Locations

Birmingham

University of Alabama, Birmingham, Alabama, United States, 35233

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility 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
  • * None, apart from not meeting Inclusion Criteria

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Varian, a Siemens Healthineers Company,

Study Record Dates

2031-12-31