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NCT06465966Active, not recruiting

UFPTI 2403-PR12: Real-Time Volumetric Ionizing Radiation Acoustic Imaging for In-vivo Proton Treatment Monitoring in Pencil-Beam Scanning

Source: ClinicalTrials.gov · Last updated 13 Oct 2026

Brief summary (registry, in English)

The purpose of this study is to evaluate the use of ionizing-radiation photo acoustic imaging (iRAI) for proton radiation treatment.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
11 (actual)
First submitted
14 Jun 2024
Start date
23 Sept 2024
Primary completion date
1 Sept 2027
Lead sponsor
University of Florida
NCT number
NCT06465966

What you commit to

  • Study type: Interventional
  • Participants enrolled: 11
  • From 23 Sept 2024 to the primary completion date, 1 Sept 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • A patient with a significant medical implant or hardware in the treatment area

Other

  • A patient who would not be tolerable or will feel nervous due to the sensation and coolness of the ultrasound gel appliedt to skin
  • A patient may feel uncomfortable with the modular transducer arrays contacting the skin during treatment. Each transducer array contacts a 15 cm × 15 cm area of skin, and depending on the patient's abdominal size, a minimum of two and a maximum of three such areas may be in contact. This produces a sensation of light pressure on the abdomen - comparable to a light hold on the index finger - lasting for a total of 4 minutes.

Who the study is looking for

  • Disease: Prostate cancer
  • Treatment site:
  • Prostate or prostate and seminal vesicle
  • No regional lymph node is involved
  • Patient's body weight: Patient's body weight is less than 350 lbs to consider the total weight limit that the ProteusONE treatment table and the robotic arm can operate
  • Treatment volume size: maximum size less than 15 x 15 cm in a cross-section and a thickness less than 20 cm to consider 2D transducer matrix size
  • Provision to sign the consent form and understand the non-invasiveness of iRAI
  • Patient agreement on tolerance on placing a water bag to acquire iRAI during treatment
  • Treatment modality: Proton radiation therapy with UFHPTI's ProteusONE gantry using PBS

Age in the registry: 18 years to 100 years · Sex: Male · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Univeristy of Florida Health Proton Therapy Institute
Coordinator of this site? Confirm its status
JacksonvilleUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.