AI and big data could slash radiotherapy side effects in prostate cancer
NCT ID NCT06714630
First seen Aug 26, 2026 · Last updated Aug 27, 2026 · Updated 1 time
Summary
This study explores whether artificial intelligence, combined with large-scale healthcare records, can help personalize radiotherapy for prostate cancer. By analyzing data from 15,000 patients, researchers aim to find ways to reduce damage to healthy tissue without compromising tumor control. The goal is to develop a method that could be used routinely in the NHS to improve quality of life for cancer survivors.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Artificial intelligence analysis of linked healthcare records to personalize radiotherapy
- What this could lead to
- If successful, this could enable personalized radiotherapy for prostate cancer, reducing damage to healthy tissue while maintaining cure rates, and potentially be rolled out across the NHS.
- What could go wrong
- This is an observational study using historical data, so it cannot prove cause and effect. The results may not apply to all patients or future treatments, and the AI models may not be accurate enough for clinical use.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 15,000 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2024
- Expected to finish
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Sep 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
This study requires no new data to be acquired relying solely on data collected on previously treated prostate cancer patients.
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
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Male participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * External beam radiotherapy delivered by a linear accelerator * Prostate Specific Antigen (PSA) recorded at regular intervals after radiotherapy * Minimum of 10 year survival post-radiotherapy * Diagnostic Computerised Tomography (CT) acquired * Radiotherapy planning CT acquired * Radiotherapy treatment planning data available * Corresponding healthcare data available to infer toxicity events (ref previous work by Lemanska et al) Exclusion Criteria: * Incomplete course of radiotherapy * No PSA data * No follow-up corresponding healthcare data available * No imaging data available
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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University of Edinburgh
RECRUITINGEdinburgh, Lothian, EH4 2XU, United Kingdom
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Steam therapy vs. surgery: can a less invasive fix help men with blocked urine flow?
- Can smart fluid monitoring improve robotic prostatectomy outcomes?
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