Skip to main content
OpenTrials
Recruiting

NCT Number: NCT07832617

Protoacoustic Imaging For 3D Mapping

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.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

OU Health Stephenson Cancer Center

Oklahoma City, Oklahoma, 73117, United States

Location status: Recruiting

Location contact

Yong Chen, PhD

CONTACT

[email protected]

405-271-3016

About this study

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.

Who can participate

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Radiacoustic Imaging w/Ultrasound.

Device

A robotic arm will position the ultrasound matrix array on the lower abdomen.

Primary outcomes

  1. Percentage of Liver Cancer Patients With Successful Respiratory Motion From Radiacoustic Imaging Tracking.

    Time frame: 1 year

    The dual-modality Radioacoustic Imaging integrated with Ultrasound (RAI/US) system in liver cancer patients is deployed to track respiratory motion, overlay real-time dose maps on ultrasound anatomy, and integrate adaptive feedback into the treatment workflow.

Secondary outcomes

  1. Percentage of Completed Workflow Treatment Plans Using Radiacoustic Imaging With Ultrasound In Prostate Cancer Patients.

    Time frame: 1 year

    Successfully develop a time-efficient RAI/US workflow for daily prostate cancer treatments, monitoring both intra- and inter-fractional motion, and applying geometric corrections to support adaptive planning.

Study contacts

Contact information is provided by the study sponsor or research team.

Lead Onco Nurse

CONTACT

[email protected]

(405) 271-3016

Yong Chen, PhD

CONTACT

[email protected]

(405) 271-3016

Sponsors and collaborators

Lead sponsor

University of Oklahoma

Other

Registry information

Official study title

Protoacoustic Imaging for 3D Mapping the Bragg Peak in Real Time During Proton Therapy (PROTEUS)

Important dates

Study start
2026
Primary completion
2028
Study completion
2030
First posted
Sep 22, 2026
Registry last updated
Sep 22, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.