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Clinical Trial ● Currently Recruiting Non-phase study NCT06280781

Imperial Prostate 9 – ATLAS (Approaches To Long-Term Active Surveillance)

Imperial Prostate 9 – ATLAS (Approaches To Long-Term Active Surveillance) — Recruiting • Non-phase study • Oncology • NCT06280781.

📅 30 Mar 2026 ⏱ 2 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
Phase
Non-phase study
NCT ID
NCT06280781
Sponsor
Imperial College London
Start
2024-05-24
ClinicaliQ Trial Snapshot
  • Imperial Prostate 9 – ATLAS (Approaches To Long-Term Active Surveillance) — Recruiting • Non-phase study • Oncology • NCT06280781.
  • The goal of this intervention study is for patients on active surveillance for prostate cancer, to demonstrate that use of regular MRI scans is better able to detect cancer progression over 5 years compared to the current NICE defined strategy. Research Question….
  • Sponsor: Imperial College London.

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What This Trial Is Studying

The goal of this intervention study is for patients on active surveillance for prostate cancer, to demonstrate that use of regular MRI scans is better able to detect cancer progression over 5 years compared to the current NICE defined strategy. Research Question P - In patients who are on active surveillance for low to medium risk prostate cancer, I - is the use of regular MRI scans C - compared to current NICE defined standard of care, O - better at detecting cancer progression with less cost to the NHS…

Eligibility Snapshot
  • : * Age 18 years or above (no upper limit) * Patients with a prostate (either cis-male gender or trans-female gender with no prior androgen deprivation hormone use at all). * Diagnostic bi-parametric or multiparametric MRI * Diagnostic systematic biopsy +/- targeted biopsy * A histological diagnosis of localised prostate cancer * Patient chosen active surveillance

Use the source registry for the full inclusion and exclusion criteria before discussing referral or enrolment.

Full Trial Details
View this trial on the source registry
Eligibility criteria, protocol, and results when available
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