Ovarian Cancer Clinical Trial
Imaging Study on Halcyon 4.0 System for Patients Receiving Radiation Therapy
Summary
This prospective imaging study is evaluating the feasibility of using the Halcyon 4.0 radiotherapy system for radiation therapy planning in patients with cancer. The Halcyon 4.0 system has been engineered to decrease the image acquisition time and the radiation exposure, but the system has not yet been clinically validated for use in radiation planning. This pilot study will evaluate images obtained on the Halcyon 4.0 system to assess if the quality is sufficient for radiation treatment plan construction.
Eligibility Criteria
Eligibility Criteria:
Planning to receive radiation therapy to one of the following sites:
Head and neck/brain (n=10)
Thorax (n=10)
Abdomen (n=10)
Pelvis (n=10)
At least 18 years of age
If the patient will be receiving IV contrast on study: Adequate renal function as defined by a serum creatinine < 1.4, or, for patients with chronic kidney disease, a stable serum creatinine < 2.0. Note: if no IV contrast will be administered on study, patient may enroll without creatinine level documented.
If the patient is a woman of childbearing potential, a negative pregnancy test must be obtained. Contraceptive use is not an adequate documentation of no chance of pregnancy.
Able to understand and willing to sign an IRB approved written informed consent document.
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There is 1 Location for this study
Saint Louis Missouri, 63110, United States More Info
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