Vascular Optimized Radiotherapy for Prostate Cancer and Erectile Function

This study is testing a special type of radiation therapy called neurovascular sparing stereotactic body radiation therapy (SBRT) for men with prostate cancer. SBRT uses highly focused X-rays to treat the cancer in five high doses. The goal is to protect the nerves and blood vessels around the prostate that are important for erectile function, as these can sometimes be affected by standard radiation. Researchers will measure sexual function using a questionnaire (EPIC-26) 24 months after treatment to see how well this technique works. You may be able to join if you are a man aged 18 or older with confirmed, localized prostate cancer. The study plans to enroll 200 participants, but its current recruitment status is unclear.

Study design
This is an interventional study planning to enroll 200 male participants aged 18 and older.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Your sexual function will be measured 24 months after treatment.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07293585

Vascular Optimized Radiotherapy Tuned to Critical Structures for Erectile Function Using High-Precision X-Ray Treatment

Recruiting
PHASE3Ages 18+InterventionalTreatment
Jonsson Comprehensive Cancer Center
~200 participants
Updated 2025-12-19 on ClinicalTrials.gov
What's tested:Neurovascular sparing stereotactic body radiation therapy

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Expanded Prostate Cancer Index Composite (EPIC-26) sexual function Questionnaire
Measured over 24 months
Prostate Cancer
1 sites across 1 states
California1
  • Amar Kishan, MD · PRINCIPAL_INVESTIGATOR · UCLA / Jonsson Comprehensive Cancer Center

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  • Expanded Prostate Cancer Index Composite (EPIC-26) sexual function Questionnaire24 months

    The primary endpoint is clinically relevant (≥24 point) decline in EPIC-26 sexual function domain scores at 24 months following treatment in patients randomized to NV-sparing SBRT relative to patients randomized to conventional SBRT without explicit NV-sparing.