HyperArc Registry Study

Status Recruiting

Clinical 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.

Clinical Trial Description

A significant percentage of newly diagnosed cancer patients will develop brain metastases. For many of these patients, stereotactic radiosurgery (SRS) is recommended as a primary treatment option. Concerns about complexity, patient safety, cost, and human resources can make SRS challenging. HyperArc radiotherapy addresses these challenges by introducing key technology and workflow elements to streamline multi-leaf collimator-based, non-coplanar SRS. HyperArc is designed to deliver SRS treatments from the TrueBeam linear accelerator platform. 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 Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05270707
Study type	Observational [Patient Registry]
Source	Varian, a Siemens Healthineers Company
Contact	Lawrence MacDonald, PhD
Phone	2066129290
Email	HyperArcRegistry@varian.com
Status	Recruiting
Phase
Start date	March 31, 2022
Completion date	December 31, 2031

View Details

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