The PROSECCA Study, Answering New Questions in Prostate Cancer

NCT06714630 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 15000

Last updated 2025-08-26

No results posted yet for this study

Summary

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.

Conditions

Sponsors & Collaborators

  • NHS Greater Glasgow and Clyde

    collaborator OTHER
  • NHS Grampian

    collaborator OTHER_GOV
  • NHS Highland

    collaborator OTHER
  • NHS Tayside

    collaborator OTHER_GOV
  • University of Glasgow

    collaborator OTHER
  • University of Lyon

    collaborator OTHER
  • NHS Lothian

    collaborator OTHER_GOV
  • NHS Research Scotland

    collaborator OTHER
  • Public Health Scotland

    collaborator UNKNOWN
  • Prostate Cancer UK

    collaborator OTHER
  • Movember Foundation

    collaborator OTHER
  • University of Edinburgh

    lead OTHER

Principal Investigators

  • Bill Nailon · University of Edinburgh

  • Duncan McLaren · University of Edinburgh

Eligibility

Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-07-01
Primary Completion
2027-09-30
Completion
2028-09-30

Countries

  • United Kingdom

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06714630 on ClinicalTrials.gov