Clinical trial · Interventional
Investigator Initiated Trial to Further Evaluate the Safety and Efficacy of Trans-perineal Focal Laser Ablation of Localized Prostate Cancer Using High Frequency Micro-ultrasound Imaging
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): Business decision of the Sponsor
Summary
Brief summary (as posted)
Trans-perineal focal laser ablation represents a promising alternative focal therapy option for patients with low-risk or favorable intermediate risk prostate cancer. FLA has been extensively utilized for over a decade in the treatment of PCa using different anatomical approaches. The proposed study differs from past ones in that a trans-perineal approach with reduced risk of infection will be used in contrast to the current trans-rectal approach. In addition, high frequency micro-ultrasound imaging will be used to enhance imaging and facilitate accurate needle placement and FLA of the index lesions. The aim of this study is to evaluate FLA as a potential optimal therapeutic intervention based on safety, ease of use, efficacy, and cost.1 FLA holds promise for the management of localized tumors. The combination of the trans-perineal focal laser ablation and micro-ultrasound imaging will enable targeted trans-perineal fusion laser induced thermal therapy of prostate cancer lesions. This approach offers significant potential advantages over traditional interventions including: * Improved dynamic ultrasound imaging of the lesion to be treated compared to traditional ultrasound techniques. * Enhanced ability to visualize and spare critical structures within the prostate, including the bladder neck, neurovascular bundle (NVB), urethral sphincter and organs in close proximity including the rectum. * Sparing these structures should translate into improved preservation of ejaculation, limited changes in sexual function and minimal transient incontinence following treatment.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Low-risk or Favorable Intermediate Risk Prostate Cancer Who Are on an Active Surveillance Regimen | — | UNRESOLVED | — |
| Prostate Cancer | Malignant Prostate Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| TRANBERG®|Thermal Therapy System | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Laser Ablation
- description
- TRANBERG® Transperineal Micro Ultrasound guided laser ablation of Prostate Cancer.
- interventionNames
- Device: TRANBERG®|Thermal Therapy System
Primary outcomes (1)
- measure
- Safety and Tolerability: Number of Adverse Events Related to the Treatment
- timeFrame
- 12 months
- description
- AE and SAE will be evaluated during all visits using the CTCAE scale. Grade 3 or greater AEs based on the CTCAE v5.0 within 5 days post procedure will be considered severe and related to the study procedure.
Secondary outcomes (1)
- measure
- Efficacy: Extent of Tumor Ablation by Laser Application
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- Male
- Minimum age
- 40 Years
- Maximum age
- 85 Years
Show eligibility criteria text
Inclusion Criteria: 1. Men between the ages of 40 and 85 years 2. Ability to read, understand and agree/sign the patient informed consent in the English language. 3. Serum PSA \< 20 ng/ml 4. AJCC clinical tumor stage T2b or less (according to digital rectal examination) 5. Men with localized PCa (GG 1or 2, Gleason Score 7 or less) (Low or Favorable Intermediate Risk PCa) with an MR-image detected index lesion done within three months from the time of enrollment and visible on micro-ultrasound 6. According to the decision of the investigator: * Patient is suitable to undergo treatment with FLA * Able to tolerate a procedure under local anesthesia * Able to undergo Nitrous Oxide sedation * Able to undergo MR * has normal rectal anatomy 7. Lesion Specificity: * Unilateral, with cumulative lesion volumes not comprising more than 50 percent of the lobe as determined by MRI * Lesion distances from the outer perimeter of the energy emitting zone of the diffuser to adjacent vital structures (bladder wall, rectal wall, neurovascular bundles, and urethra) must be ≥ 8mm 8. Minimum distance to rectal wall and other sensitive structures ≥ 8mm Exclusion Criteria: 1. Previous prostate surgery 2. Patients with recurrent prostate cancer 3. Anticoagulant therapy 4. Gleason Grade Group 3 PCa or higher 5. Multifocal PCa other than Gleason Grade Group 1 6. Locally advanced or metastatic PCa 7. Prior or ongoing PCa treatment including surgery, radiation therapy, hormonal therapy or focal therapy 8. Previous radiation of the pelvic region 9. Intraprostatic calculus \> 5mm 10. Inability to tolerate a dorsal lithotomy position under Nitrous Oxide sedation for \> 90 minutes 11. ECOG Status ≥2 12. Urethral Stenosis 13. Prostate height \> 5 cm anterior to posterior or a prostate volume \>100 cc's
References
Publications (1)
- BACKGROUNDKayano PP, Klotz L. Current evidence for focal therapy and partial gland ablation for organ-confined prostate cancer: systematic review of literature published in the last 2 years. Curr Opin Urol. 2021 Jan;31(1):49-57. doi: 10.1097/MOU.0000000000000838. PMID 33196540