Can a shorter radiation course for prostate cancer be just as safe?
NCT ID NCT05820633
First seen Jun 25, 2026 · Last updated Jun 26, 2026 · Updated 1 time
Summary
This phase 3 trial compares a new, shorter course of radiation (ultra-hypofractionated) to the standard longer course for men with prostate cancer that has spread to lymph nodes. Both groups also receive a brachytherapy boost and hormone therapy. The study aims to see if the shorter treatment causes similar side effects and maintains quality of life. 500 participants are planned, but the trial is currently suspended.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Radiotherapy (ultra-hypofractionated pelvic IMRT with HDR brachytherapy boost)
- What this could lead to
- If successful, this could show that a shorter course of radiation is just as safe and effective as the standard longer course for prostate cancer patients.
- What could go wrong
- This trial is currently suspended, so results may be delayed or not happen. It is a non-inferiority study, meaning it aims to prove the new approach is not worse than the standard, not necessarily better. Side effects from radiation remain a risk.
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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About 500 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2022
- Expected to finish
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Dec 2035
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.
- Ages
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18 to 95 years
- 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: * Histopathologically confirmed adenocarcinoma of the prostate. * All clinical stages with lymph node involvement risk needing pelvis RT. * Stage Mx or M0. * Unfavorable Intermediate, high or very high-risk disease according to NCCN guidelines. * Having the ability to give free and informed consent. Exclusion Criteria: * Clinical stage M1. * IPSS Score \> 20 with alpha-blocking medication. * Prior pelvic radiotherapy, * History of active collagenosis (Lupus, Scleroderma, Dermatomyositis). * Past history of Inflammatory Bowell Disease. * Bilateral hip prosthesis.
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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
11 sites. The list below names each one and where it is.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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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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BC Cancer Sindi Ahluwalia centre for the Southern Interior
Kelowna, British Columbia, V1Y 5L3, Canada
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CHU de Québec - Université Laval
Québec, G1R 2J6, Canada
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CISSS de Laval, Hôpital de la Cité-de-la-Santé
Laval, Quebec, H7M 3L9, Canada
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CISSS de l'Outaouais, Hôpital de Gatineau
Gatineau, Quebec, J8P 7H2, Canada
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CISSS de la Montérégie-Centre, Hôpital Charles-Le Moyne
Longueuil, Quebec, J4V 2H1, Canada
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CIUSSS de l'Est-de-l'Île-de-Montréal, Hôpital Maisonneuve-Rosemont
Montreal East, Quebec, H1T 2M4, Canada
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CIUSSS de l'Estrie - Centre Hospitalier Universitaire de Sherbrooke (CHUS)
Sherbrooke, Quebec, Canada
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CIUSSS du Centre-Ouest-de-l'Île-de-Montréal, Jewish General Hospital
Montreal, Quebec, H3T 1E2, Canada
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Carlo Fidani Peel Regional Cancer Centre
Mississauga, Ontario, L5M 2N1, Canada
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Cedars Cancer Centre, McGill University Health Centre (MUHC)
Montreal, Quebec, H4A 3J1, Canada
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Lakeridge Health Oshawa Cancer centre
Oshawa, Ontario, L1G 2B9, Canada
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- A scanner in the operating room could show surgeons exactly where prostate cancer remains
- New PET tracer aims to light up hidden cancer targets
- Can daily adaptive radiotherapy spare healthy tissue in prostate cancer?
- Can a radioactive tracer and MRI reveal prostate Cancer's true extent?
- Five-Fraction radiation plus hormone therapy tested against High-Risk prostate cancer
- Can a 10-Hour eating window fight cancer fatigue?