Clinical trial Recruiting at 1 site Observational Ages 18 and up

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.

More Prostate Cancer trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment24 (estimated)
SponsorUniversity of Oklahoma
Academic / other
Drugs / interventionsradiation
Locations1 site (Oklahoma City, Oklahoma)
StatusRecruiting
StartedJune 10, 2026
Main results expectedJune 2028
Study endsJune 2030
Registry record updatedSeptember 22, 2026
Trial IDNCT07832617 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

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.