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NCT07832617Recruiting

Protoacoustic Imaging For 3D Mapping

University of Oklahoma

Start Date

6/10/2026

Completion Date

6/1/2030

Summary

The purpose of this study is to test a new imaging technology called radioacoustic imaging (RAI) that may help doctors see where radiation is being delivered during proton therapy. During proton therapy, the radiation treatment produces very small sound signals inside the body. This study will use special ultrasound sensors placed on the outside of the body to detect these signals. The information collected may allow researchers to create a picture showing where the radiation dose is being delivered in the body and how much radiation is reaching the treatment area. The goal is to determine whether this technology can safely and accurately measure radiation during proton therapy without requiring any additional procedures or radiation exposure.

Detailed Description

Radiation therapy is a cornerstone of cancer treatment, and proton therapy offers enhanced precision for treating deep-seated tumors due to the Bragg Peak phenomenon, which allows for concentrated dose delivery while minimizing exposure to surrounding healthy tissue. This study seeks to build upon this advantage by incorporating real-time, in vivo verification of proton dose deposition. The study hypothesizes that integrating RAI with ultrasound (US) will enable real-time dose verification and motion tracking, thereby improving the accuracy, adaptability, and overall effectiveness of proton therapy for moving targets such as the liver and prostate. Participants enrolled in the study will first undergo standard X-ray alignment as part of their routine treatment workflow. Following alignment, a robotic arm will position an ultrasound matrix array over the lower anterior abdominal region. A conformal, water-mediated interface in combination with ultrasound gel will be used to ensure optimal acoustic coupling between the transducer and the patient's skin, allowing for passive detection of acoustic signals generated during proton beam delivery. These signals will be used to reconstruct and monitor dose deposition in real time throughout treatment.

Eligibility Criteria

Age Range: 18 years to No maximum

Inclusion Criteria: * Patients at least \>18years old * Patients referred to OUHSC SCC for SOC PT * Patients receiving treatment for indications where RAI data collection is feasible (e.g., liver and prostate) * Willingness and ability to provide a documented informed consent Exclusion Criteria: * Patients with contraindications for ultrasound coupling (e.g., extensive open wounds or skin conditions at transducer placement sites). * Patients whose treatment plan or setup prevents the practical application of the RAI system without interfering with standard clinical care * Patients with implanted electronic devices (e.g., pacemakers) in the treatment region if there is any concern of device interference, even though the RAI system is passive.

Interventions

DEVICE

Radiacoustic Imaging w/Ultrasound.

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Conditions

Proton TherapyRadiation Therapy, Secondary Skin ReactionsLiver CancerProstate Cancer

Locations

OU Health Stephenson Cancer Center

Oklahoma City, Oklahoma 73117

United States