MRI or CT planning to guide high-dose-rate prostate brachytherapy
Official title: A Randomized Pragmatic Study of CT- Versus MRI-Based Planning for High-Dose-Rate Prostate Brachytherapy for Prostate Cancer
Run by Emory University · NCT07859722 · Data updated 2026-11-12
This trial tests whether adding an MRI to CT-based treatment planning for HDR prostate brachytherapy changes urinary side effects in men with localized prostate cancer.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | Men only |
| Enrollment | 100 (estimated) |
| Sponsor | Emory University Academic / other |
| Drugs / interventions | radiation |
| Locations | 3 sites (Atlanta, Georgia and 2 other locations) |
| Status | Recruiting |
| Started | October 22, 2026 |
| Main results expected | May 31, 2028 |
| Study ends | May 31, 2029 |
| Registry record updated | November 2, 2026 |
| Trial ID | NCT07859722 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Men aged 18 or older with histologically confirmed localized prostate cancer (stages I–III) planned for curative HDR brachytherapy, with no prior pelvic radiation or prostate MRI, and no metastases.
✕Probably not a fit
Patients without MRI-visible benefits or with risk profiles not influenced by MRI planning may see no difference in outcomes.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This interventional study randomizes men with localized prostate cancer to HDR brachytherapy planning using CT alone or CT with an MRI. The primary aim is to see if adding MRI affects acute urinary toxicity as measured by EPIC-26 urinary incontinence scores. Secondary goals include longer-term urinary irritative/obstructive symptoms, bowel and sexual domains, and physician-reported toxicity (CTCAE) for both acute and chronic periods. The trial follows participants for 12 months after treatment to compare outcomes and explore treatment efficacy between the two planning approaches.
Why it matters
Potential benefit: If MRI planning improves toxicity profiles, patients may experience fewer urinary or bowel side effects after HDR brachytherapy.
How similar studies have gone: Previous work in imaging-guided planning suggests potential for improved toxicity outcomes with MRI, but direct randomized data for HDR prostate brachytherapy planning remain limited.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Men ≥ 18 years old * Histopathologically confirmed prostate cancer * No evidence of regional or distant metastases * Plan to undergo curative-intent HDR brachytherapy with or without external beam radiation therapy Exclusion Criteria: * Prior pelvic radiation therapy * No prior prostate MRI
Where it's running
-
Emory Proton Therapy Center
Atlanta, Georgia, United States Recruiting -
Emory University Hospital Midtown
Atlanta, Georgia, United States Recruiting -
Emory University Hospital/Winship Cancer Institute
Atlanta, Georgia, United States Recruiting
Study contacts
- Principal investigator: Kamran Salari, MD — Emory University Hospital/Winship Cancer Institute
- Study coordinator: Kamran Salari, MD
- Email: kamran.salari@emory.edu
- Phone: 404-686-2391
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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.