Empty bladder may ease prostate radiation prep, trial suggests
NCT ID NCT06037863
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This trial tests whether having an empty bladder before CT simulation for prostate cancer radiation therapy is better than the usual full bladder. The goal is to see if it reduces urinary symptoms and makes daily treatments more consistent. About 168 men with prostate cancer will be randomly assigned to either empty or full bladder preparation.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- bladder filling procedure
- What this could lead to
- If it works, this could show that an empty bladder is just as good or better for radiation planning, reducing patient discomfort and treatment delays.
- What could go wrong
- This is a small, early-stage trial (168 participants) comparing two preparation methods, not a new treatment. Results may not change standard practice or apply to 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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168 people
The number who actually took part.
- Started
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Sep 2023
- Expected to finish
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Dec 2027
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 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.
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: * Age \>= 18 years * Histological confirmation of prostate cancer * Planned definitive dose radiotherapy to the prostate * Note: Patients are eligible for enrollment if they are already enrolled or planned for enrollment on another interventional research protocol provided that other study protocol treatment does not require procedures or treatments that would be in conflict with the eligibility or treatment protocols for this study nor, in the judgement of the enrolling physician, affect primary study objectives of this study * Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0, 1, or 2 * Ability to complete questionnaire(s) by themselves or with assistance * Provide written informed consent Exclusion Criteria: * Planned delivery of radiotherapy to pelvic lymph nodes * Planned brachytherapy treatment of the prostate * Significant urinary incontinence that precludes standard bladder filling * Evidence of direct bladder extension or bladder wall metastases from prostate cancer * Used indwelling or intermittent urinary catheterization at baseline * Prior pelvic radiotherapy such that any portion of the prostate received \> 5 Gy
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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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Mayo Clinic Health System in Albert Lea
Albert Lea, Minnesota, 56007, United States
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Mayo Clinic Health System-Eau Claire Clinic
Eau Claire, Wisconsin, 54701, United States
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Mayo Clinic Health System-Franciscan Healthcare
La Crosse, Wisconsin, 54601, United States
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Mayo Clinic Health Systems-Mankato
Mankato, Minnesota, 56001, United States
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Mayo Clinic in Arizona
Scottsdale, Arizona, 85259, United States
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Mayo Clinic in Florida
Jacksonville, Florida, 32224-9980, United States
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Mayo Clinic in Rochester
Rochester, Minnesota, 55905, United States
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Other studies related to the condition(s) this trial covers.
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