Lower Urinary Tract Symptoms Clinical Trial
Official title:
Registry of Transperineal Laser Ablation for Treatment of Lower Urinary Tract Symptoms With Use of the Echolaser® Device: A Multicentre, International Registry to Evaluate the Treatment of LUTS in Terms of Long-term Efficacy, Functional Outcomes and Safety
Rationale: The treatment of lower urinary tract symptoms (LUTS) due to benign prostatic
enlargement in men with transperineal laser ablation (TPLA) may offer advantages in
functional outcomes and safety over current standard therapies. As the technique is
relatively new, indications and outcomes for this treatment are subject of investigation.
However, the technique is already applied outside clinical studies. Clinical information from
these treatments can be useful for future research. The aim of this study is to collect data
on patients treated with transperineal laser ablation of the prostate outside clinical trials
and to provide data on safety and functional outcomes in these patients in order to improve
treatment.
Objective: To assess long-term efficacy of transperineal laser ablation for lower urinary
tract symptoms, to assess functional outcomes, to assess safety, to determine baseline
patient characteristics, to collect information on possible differences between centres
applying treatment of transperineal laser ablation and to explore the optimal treatment
indications and possible limitations.
Study design: This is an international prospective observational study in which data is
recorded of patients who are treated with transperineal laser ablation for lower urinary
tract symptoms.
Study population: Male patients treated with transperineal laser ablation for lower urinary
tract symptoms due to benign prostatic enlargement.
Main study parameters/endpoints: The primary endpoint of this study is long-term efficacy of
transperineal laser ablation for lower urinary tract symptoms measured by the time until
surgical retreatment.
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