ArticleCureus2025
Histoblast: A Novel Cavitative High-Intensity Focused Ultrasound (HIFU)-Modified Technique for Benign Prostatic Hyperplasia.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07757490 (SONAFUSION Registry), which is not on this map. Not yet cited in PubMed.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
SONAFUSION Registry (Long-term Evaluation of Sonablate High-Intensity Focused Ultrasound for the Treatment of Prostate Cancer and Benign Prostatic Hyperplasia)
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Benign prostatic hyperplasia (BPH) is a prevalent condition, often requiring intervention due to its impact on quality of life. High-intensity focused ultrasound (HIFU) has demonstrated efficacy in prostate cancer treatment; however, its application in BPH remains limited by prolonged treatment times and delayed symptom relief. This report introduces a novel HIFU-based technique (Histoblast) using the Sonablate 500® (SB-500) system to improve treatment efficiency and clinical outcomes in BPH. Key modifications to the conventional HIFU approach include: (1) a checkerboard treatment pattern to reduce treatment time (TT) and tissue edema; (2) prostate compression via increased degassed water volume to minimize heat dissipation and enhance acoustic efficiency; and (3) optimized energy delivery within the upper third of the device's approved range. Treatment progress is monitored using standard safety parameters, including Tissue Change Monitoring and Reflectivity Index measurements. The procedure is performed under spinal anesthesia, with postoperative catheterization lasting approximately four days. This technique reduces the number of treatment shots by 40-50%, achieving a significantly shorter TT. Controlled acoustic cavitation is observed in up to 70-75% of treated zones, indicating effective tissue ablation. Preservation of the urethra and bladder neck is prioritized to facilitate early catheter removal. This technique represents a promising refinement of HIFU for BPH management and warrants further clinical evaluation.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.