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The PROSECCA Study, Answering New Questions in Prostate Cancer

Sponsor: University of Edinburgh

NCT ID: NCT06714630

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Health checks and monitoring — no treatment given
Type of study
Observational (no treatment given)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
Not specified by the sponsor
How long the study runs
Study runs about 50 months (dates as stated)
About the drug or intervention
Not specified by the sponsor
Patient visit burden
Not specified by the sponsor

In plain English

This study, run by the University of Edinburgh, looks back at men who had radiotherapy for prostate cancer delivered by a machine called a linear accelerator. Researchers will use old scans, treatment records and health data to answer new questions about prostate cancer. No new treatment is given as part of this study.

Who can take part

  • Radiotherapy given by a machine called a linear accelerator
  • Blood test results (PSA, or prostate specific antigen) recorded regularly after radiotherapy
  • At least 10 years of survival after radiotherapy
  • A diagnostic CT (computerised tomography) scan taken
  • A planning CT scan taken for the radiotherapy
  • Radiotherapy treatment planning data available
  • Health records available that show any side effects

Who may not be able to

  • Did not complete the course of radiotherapy
  • No PSA blood test data
  • No follow-up health records available
  • No imaging data available

What taking part involves

  • • Not stated — ask the trial team. This study appears to use existing records and scans rather than giving treatment.

Time commitment: Not stated — ask the trial team; the study uses existing scans, treatment data and health records collected after radiotherapy.

Plain-English summary (AI-generated) from registry data. Not eligibility advice — only the trial team can confirm whether you can take part. Use the eligibility checker to see how your health profile matches this trial.

Type of study
Observing health over time
Ages
Not specified
Who
Male
Number of participants
15,000
Started
2024-07-01
Last checked
2026-08

Plain English Summary

What is this study?

  • • Testing a new treatment for prostate cancer
  • • Clinical study - 15,000 participants
  • • Nearly half of all cancer patients receive radiotherapy as part of their treatment and although it is effective at destroying cancerous lesions deep within the body, this comes at the cost of damaging healthy, or normal, tissues

Who can take part?

  • • Adults
  • • Diagnosed with prostate cancer
  • • Male only

Where?

  • • Edinburgh - University of Edinburgh

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

Nearly half of all cancer patients receive radiotherapy as part of their treatment and although it is effective at destroying cancerous lesions deep within the body, this comes at the cost of damaging healthy, or normal, tissues. With 50% of cancer patients surviving for 10 years or more, these patients can be left with life-changing side effects from their radiotherapy. It is clear that more must be done to limit damage to normal healthy tissue without compromising annihilation of the tumour and curing patients. The key to this is personalising an individual's radiotherapy treatment, in other words rather than assuming that all tumours respond similarly to radiotherapy, the treatment is optimised for an individual. To date, approaches to do this have been restricted to small numbers of carefully selected patients, are inordinately expensive, and not suitable for rolling out into everyday practice across the NHS. There is however another way, namely using Artificial Intelligence (AI) combined with an individual's healthcare record. By linking together large numbers of healthcare records at a national level, combined with the power of AI, the PROSECCA project will transform radiotherapy and cancer care.

More detail

As an example of how this technology is beginning to emerge, proof of concept data from the team has shown that using AI it is possible to identify patients at increased risk of damage from radiotherapy long before they receive any radiation as part of their treatment. However, to move these AI-based approaches from the research domain into the clinic requires significant effort, which is the aim of PROSECCA study. The project will use AI to analyse healthcare records from up to 15,000 prostate cancer patients who underwent radiotherapy in Scotland. Through linkage of data obtained specifically for radiotherapy and data held within each patient's unique healthcare history it will be possible to establish new relationships between a patient's medical history and how well a patient responds to radiotherapy. By establishing what factors or information in a patient's complex healthcare record indicate that an individual may have a poor response to treatment, or an increased risk of side effects from radiation, it will be possible to identify these patients earlier than is currently possible and adapt treatment accordingly. Furthermore, identifying these important factors would improve radiotherapy treatment for prostate cancer patients in the future.

Prostate Cancer

How this trial compares with your answers

Answer 2 more questions to improve match

What we know so far

Condition· Matched your search
Age· Tell us your age for better matching
Gender· Tell us your sex for better matching

Still need:

  • • Tell us your age for better matching
  • • Tell us your sex for better matching

Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: Not specified
  • Who can join: Male only

Biomarkers mentioned

PSA

What the study is looking for

  • ✓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

Who cannot take part

  • ✗Incomplete course of radiotherapy
  • ✗No PSA data
  • ✗No follow-up corresponding healthcare data available
  • ✗No imaging data available
See the full criteria
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

Where Is This Study? (1 UK site)

University of Edinburgh

Edinburgh EH4 2XU, United Kingdom

Recruiting
Site contact (verified)

How to Get in Touch

Bill Nailon

Sponsor contact

CONTACT

0044 1315371000 w.nailon@ed.ac.uk

Duncan McLaren

Sponsor contact

CONTACT

0044 1316518706 Duncan.McLaren@ed.ac.uk
Data sourced from ClinicalTrials.gov · Last verified: 2026-08