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Transperineal Laser Ablation for Percutaneous Treatment of Benign Prostatic Hyperplasia

Lower Urinary Tract Symptoms Clinical Trial

Official title:
Transperineal Laser Ablation for Percutaneous Treatment of Benign Prostatic Hyperplasia: A Feasibility Study - Results at 6 and 12 Months From a Retrospective Multi-centric Study

Clinical Trial Summary

This study investigated the effectiveness and safety of SoracteLite ™- Trans-Perineal Laser ablation (TPLA) in the treatment of patients with symptomatic Benign Prostatic Hyperplasia (BPH) at 6 and 12 months follow-up

Clinical Trial Description

The purpose of this study was to investigate the effectiveness and safety of SoracteLite ™ - Trans-Perineal Laser ablation (TPLA) in the treatment of patients with symptomatic benign prostatic hyperplasia (BPH) at 6 and 12 months follow-up. Methods: Patients with urinary symptoms secondary to BPH underwent TPLA under local anaesthesia in four centers. Under US guidance, up to four 21G applicators were inserted in the prostatic tissue. Each treatment was performed with diode laser operating at 1064 nm changing the illumination time according to prostate size. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04198103
Study type Interventional
Source University of Rome Tor Vergata
Contact
Status Active, not recruiting
Phase N/A
Start date November 1, 2018
Completion date March 1, 2020
View Details
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