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Precision radiation for prostate cancer shows promise in early trial

NCT ID NCT02470897

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 26, 2026 · Last updated Jun 26, 2026

Summary

This study tested a new way to deliver radiation for prostate cancer. The goal was to give a higher dose to the tumor while protecting the urethra and other healthy tissue. 115 men with early-stage prostate cancer took part. The researchers looked at side effects and how well the treatment worked over time.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
radiation therapy (SBRT with IMRT planning)
What this could lead to
If successful, this approach could offer a shorter, more precise radiation treatment for prostate cancer with fewer side effects.
What could go wrong
This is an early-phase study focused on safety and dosing, so it's not yet proven to be better than standard radiation. There is still a risk of urinary or rectal side effects.

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

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

115 people

The number who actually took part.

Started

Jul 2015

Finished

Aug 2025

Lead sponsor

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

Children (under 18), adults (18 to 64) and older adults (65 and over)

Sex

Male participants only

Healthy volunteers

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

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 diagnosis of adenocarcinoma of the prostate and most recent biopsy within 180 days of study enrollment * History/physical examination with digital rectal examination of the prostate within 90 days prior to study enrollment * Gleason score =\< 7, no tertiary pattern \>= 5 * Clinical stage =\< T2b (American Joint Committee on Cancer \[AJCC\] 7th Edition Staging Manual) and no radiographic evidence of T3 or T4 disease * Clinical stage N0, M0 * Most recent prostate specific antigen (PSA) within 60 days of enrollment * Maximum PSA =\< 20 ng/ml (not within 20 days after biopsy) * Eastern Cooperative Oncology Group (ECOG) performance status 0-1 * American Urological Association (AUA) =\< 18 with or without medical management * Up to a total of year of androgen deprivation allowed. * Participant signs study specific informed consent prior to study enrollment Exclusion Criteria: * FOR ARM A: Inability to obtain a planning MRI or a planning MRI of sufficient quality to allow identification of the peripheral zone and urethra, or inability to adequately fuse the MRI to the planning CT scan * FOR BOTH ARM A AND ARM B: * Prior or concurrent invasive malignancy (except non-melanomatous skin cancer) or lymphomatous/hematogenous malignancy unless continually disease free for a minimum of 5 years; (for example, carcinoma in situ of the bladder or oral cavity is permissible) * Prosthetic implants in the pelvic region that the investigator feels will impede treatment, planning, or delivery (e.g., an artificial hip) * =\< 3 months from a transurethral resection of the prostate (TURP) procedure * Significant urinary obstruction (i.e. AUA symptom score \> 18) * Previous pelvic irradiation, prostate brachytherapy * Previous radical surgery (prostatectomy) or cryosurgery for prostate cancer * Severe, active comorbidity, defined as follows: * Acute bacterial or fungal infection requiring intravenous antibiotics at the time of registration * Crohn's disease or ulcerative colitis * Scleroderma

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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

  • Swedish American

    Rockford, Illinois, 61104, United States

  • UW Cancer Center, Johnson Creek

    Johnson Creek, Wisconsin, 53038, United States

  • University of Wisconsin Carbone Cancer Center

    Madison, Wisconsin, 53792, United States

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