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NCT06925295RecruitingPhase 2

Using Xe MRI to Guide Radiation Therapy for Lung Cancer

Image-Based Functionally Adapted Radiation Therapy for Lung Cancer

Source: ClinicalTrials.gov · Last updated 2 Jan 2026

Brief summary (registry, in English)

The purpose of this research study is to explore using MRI scans with xenon to better image lung function, how lung function changes after radiation therapy, and to guide radiation therapy away from parts of the lung that have good function. This project is foundational to performing additional studies to establish if novel MRI imaging can serve as a guidance tool for lung cancer radiation treatment.

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
15 (estimated)
First submitted
28 Mar 2025
Start date
30 Aug 2025
Primary completion date
31 Jan 2027
Lead sponsor
Sean Fain
Diseases
Lung cancer
NCT number
NCT06925295

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 15
  • From 30 Aug 2025 to the primary completion date, 31 Jan 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

  • Subject has concurrent cancer treatment with agents associated with increased risk of radiation pneumonitis (e.g. immunotherapy, chemotherapy)

Other illness

  • Respiratory illness of bacterial or viral etiology within 30 days of planned treatment
  • Subject has history of any known ventricular cardiac arrhythmia
  • Subject has history of cardiac arrest within the last year
  • Subject has prior history of cancer treatment with radiation therapy to the lung
  • Medical or psychological conditions which, in the opinion of the investigator, might create undue risk to the subject or interfere with the subject's ability to comply with the protocol requirements

Age

  • Subject is less than 18 years old or incarcerated

Other

  • Subjects presenting with any of the following will not be included in the trial:
  • MRI is contraindicated based on responses to MRI screening questionnaire
  • Subject is pregnant or lactating
  • Resting oxygen saturation \<90% on supplemental oxygen
  • Subject does not fit into 129Xe vest coil used for MRI
  • Subject cannot hold his/her breath for 15 seconds
  • Subject deemed unlikely to be able to comply with instructions during imaging

Who the study is looking for

  • Subjects must meet all of the following inclusion criteria to be eligible for enrollment into the trial
  • Aged 18-80 years
  • Willing and able to provide informed consent and adhere to visit/protocol schedules (Consent must be given before any study procedures are performed.)
  • Clinical diagnosis of lung cancer made by a board-certified oncologist with intent to treat with stereotactic body radiation therapy. We will not exclude individuals based on cancer type or severity of disease with the exception of the below criteria

Age in the registry: 18 years to 80 years · Sex: All · 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
University of Iowa
Coordinator of this site? Confirm its status
Iowa CityUnited StatesRecruiting

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