HyperSight CBCT Imaging for Enhanced Radiotherapy in Cancer Patients
Comparison of HyperSight CBCT imaging to conventional CBCT imaging.
Urogenital Diseases+15
+ Breast Diseases
+ Breast Neoplasms
Other Study
Summary
Study start date: February 19, 2025
Actual date on which the first participant was enrolled.This study focuses on testing a new imaging technology called HyperSight, designed to improve the quality of images used during radiation therapy for cancer patients. Traditional cone beam computed tomography (CBCT) systems help position patients accurately for their daily treatments but often produce images with poor contrast and artifacts, limiting their usefulness for other purposes. HyperSight, developed by Varian Medical Systems, aims to overcome these limitations, potentially enhancing the overall radiation therapy process. The study's goal is to assess whether HyperSight can provide higher quality images that could assist in creating more precise radiation plans. Participants in this study will undergo imaging using the HyperSight-TrueBeam system, which utilizes a rotating C-shaped arm to capture images of different body areas. The collected images will be carefully evaluated to see if they offer better clarity and detail compared to traditional CBCT images. By measuring the quality of the HyperSight images, the study aims to determine if they can be used for more than just patient alignment, such as calculating radiation treatment plans. There are no specified risks or benefits mentioned, but the potential for improved treatment accuracy could offer significant advantages for cancer patients.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.50 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Other Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 4 locations
Ohio State University, Brain and Spine Hospital
Columbus, United StatesThe Arthur G. James Cancer Hospital and Richard J. Solove Research Institute
Columbus, United StatesStefanie Spielman Comprehensive Breast Center
Columbus, United States