Protoacoustic Imaging to See Radiation Delivery in Proton Therapy
Official title: Protoacoustic Imaging for 3D Mapping the Bragg Peak in Real Time During Proton Therapy (PROTEUS)
Run by University of Oklahoma · NCT07832617 · Data updated 2026-11-12
This study tests radioacoustic imaging with ultrasound to help doctors see where proton therapy is delivering radiation for liver and prostate cancer patients.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 24 (estimated) |
| Sponsor | University of Oklahoma Academic / other |
| Drugs / interventions | radiation |
| Locations | 1 site (Oklahoma City, Oklahoma) |
| Status | Recruiting |
| Started | June 10, 2026 |
| Main results expected | June 2028 |
| Study ends | June 2030 |
| Registry record updated | September 22, 2026 |
| Trial ID | NCT07832617 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults 18 years or older undergoing proton or radiation therapy for liver or prostate cancer where RAI data collection is feasible.
✕Probably not a fit
Patients whose treatment plan does not allow practical application of the RAI system or who have ultrasound contraindications may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study evaluates a new imaging approach called radioacoustic imaging (RAI) that uses external ultrasound sensors to detect sound signals produced by proton therapy. The goal is to create real-time visualizations of dose deposition without extra radiation exposure or procedures. Participants receive standard X-ray alignment and then have an ultrasound matrix placed over the lower abdomen to capture signals during beam delivery, aiming to verify dose accuracy and track motion. Data will assess whether RAI can safely and effectively visualize where protons deposit their energy in moving targets like the liver and prostate. No additional interventions beyond the imaging modality are required if feasible within routine care.
Why it matters
Potential benefit: If successful, this approach could provide real-time verification of proton dose delivery, potentially improving treatment accuracy and adapting to motion.
How similar studies have gone: Previous work in radioacoustic imaging for radiation verification is promising but this application to proton therapy is exploratory and not yet proven in routine care.
Who can join: the full rules
Show full inclusion / exclusion criteria
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.
Where it's running
-
OU Health Stephenson Cancer Center
Oklahoma City, Oklahoma, United States Recruiting
Study contacts
- Principal investigator: Yong Chen, PhD — University of Oklahoma - Stephenson Cancer Center
- Study coordinator: Lead Onco Nurse
- Email: SCC-IIT-Office@ouhsc.edu
- Phone: (405) 271-3016
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.