New PSMA scan aims to spot hidden prostate cancer spread
NCT ID NCT04745871
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether a special type of PET/CT scan, called PSMA PET/CT, can better detect if prostate cancer has spread to nearby lymph nodes before surgery. The scan uses a radioactive tracer that sticks to prostate cancer cells, making them visible. The goal was to help doctors plan more precise surgery for men with intermediate- or high-risk prostate cancer. However, the trial was stopped early, so we have less information than planned.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- PSMA PET/CT scan (a type of imaging test using a radioactive tracer)
- What this could lead to
- If successful, this imaging test could help doctors more accurately decide the extent of surgery needed for prostate cancer, potentially reducing unnecessary procedures.
- What could go wrong
- The trial was terminated early, so results are limited. PSMA PET/CT is still being studied and may not be widely available or better than current standard imaging for all patients.
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.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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112 people
The number who actually took part.
- Started
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May 2021
- Finished
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Nov 2025
- 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.
- Ages
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18 years and older
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Histologically confirmed prostate cancer; * Intermediate-risk prostate cancer (PSA level of 10- 20 ng/mL and/or Clinical tumor stage ≥ T2b and/or ISUP 2 or 3, AND with risk of lymph node extension \> 5% according to the Briganti nomogram) or high-risk prostate cancer (PSA ≥ 20 ng/mL and/or TR ≥ T2c and/or ISUP 4 or 5) according to d'Amico classification; * Curative treatment by radical prostatectomy chosen by the multidisciplinary consultation meeting. Exclusion Criteria: * Refusal or inability to participate in the study ; * Low-risk prostate cancer according to D'Amico's classification, or an intermediate-risk but with a risk of lymph node extension \<5% according to Briganti's nomogram; * Curative treatment other than surgical treatment chosen; * Life expectancy \< 12 months; * Karnofsky score \< 70 or ECOG score \> 2.
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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.
Contacts and locations
Locations
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CHRU de Brest
Brest, 29609, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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