Laser zaps prostate tumors in tiny study
NCT ID NCT06047509
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a new way to treat prostate cancer using a laser guided by MRI images. Only 2 men took part before the study was stopped. The goal was to see if the treatment was safe and could precisely target cancer while avoiding healthy tissue.
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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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2 people
The number who actually took part.
- Started
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Sep 2023
- Finished
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Jan 2026
- 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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40 to 85 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: * Subjects with organ-confined prostate cancer (clinical stage ≤ T2b, Gleason =7) * Age 40 to 85 years of age * Multi-parametric MRI read at study site within 9 months of study treatment, demonstrating a Region of interest (ROI) of MRI (PIRADSv2 \> Grade 3)1 * Prostate volume 20cc to 80cc * MRI/ultrasound fusion biopsy with ≥ 10 systematic biopsy cores and ≥ 2 targeted biopsy cores from above MRI-derived ROI within 6 months of study treatment\* * Histologically confirmed adenocarcinoma from targeted biopsy cores * Overall Gleason = 3+4 or 4+3 * Subjects desire focal therapy and decline conventional treatment (active surveillance, radical prostatectomy, radiation therapy, cryosurgery, and hormone therapy) * Treatment plan that allows for treatment of lesion while still maintaining a 4mm safety margin from the rectal wall and urethra * Signed informed consent for the FLA treatment through follow-up per study protocol * For subjects under consideration for repeat FLA, the post-treatment MRI and biopsies done at Months 6 and 12 study visits may be used for these criteria. Exclusion Criteria: * Any significant cancer outside of the intended treatment zone, defined as Gleason score ≥ 7 * \< 10 years life expectancy * Any medical condition that would compromise the subject's ability to safely participate in the study * Active bleeding disorder * Use of coumadin or any other anticoagulant, unless anticoagulation can be temporarily reversed or stopped for a window of at least 7 days peri-procedure * Use of aspirin, unless it can be temporarily stopped for a window of at least 14 days prior to FLA procedure * Use of NSAIDS (except aspirin), Vitamin E, multivitamins, and herbal products, unless they can be temporarily stopped for at least 7 days prior to FLA procedure * Active urinary tract infection * Active prostate abscess, prostatitis, or neurogenic bladder * Any prior treatment for prostate cancer, including: * Radical prostatectomy * Radiation therapy (external beam or brachytherapy) * Cryotherapy * High intensity focused ultrasound (HIFU) treatment * Photodynamic therapy * Androgen deprivation therapy * Focal Laser Ablation (acceptable for enrolled subjects under consideration for repeat FLA) * Prior prostate, bladder neck, or urethral stricture surgery * Any prostate debulking procedure, including transurethral resection of prostate, photovaporization, or electrovaporization * Transurethral incision of bladder neck * Urethral stricture dilation or reconstruction * Use of 5-alpha reductase inhibitors within 6 months of treatment * Prior significant rectal surgery (hemorrhoidectomy is acceptable) * Active rectal fissure, fibrosis, stenosis, or other anatomic abnormality precluding insertion of transrectal device * Active inflammatory bowel disease * Urinary tract or rectal fistula * Previous urethral sling, artificial urinary sphincter, or penile prosthesis surgery. * Any contraindication to MRI (contrast allergy, severe claustrophobia, MRI-incompatible prosthesis, MRI-unsafe aneurysm clips)
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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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UCLA / Jonsson Comprehensive Cancer Center
Los Angeles, California, 90095-1406, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Can a 10-Hour eating window fight cancer fatigue?