European Registry for Transperineal Laser Ablation of Prostate (TPLA) for Lower Urinary Tract Symptoms
Launched by UNIVERSITY OF FLORENCE · Aug 18, 2024
Trial Information
Current as of June 04, 2025
Recruiting
Keywords
ClinConnect Summary
The European Registry for Transperineal Laser Ablation of Prostate (TPLA) is a study designed to evaluate the effectiveness and safety of a laser treatment for men experiencing bothersome urinary symptoms due to an enlarged prostate, a condition known as benign prostatic hyperplasia. This treatment aims to relieve symptoms without needing further surgery. The researchers will collect information from patients about their experiences and outcomes after the procedure to understand how well it works over time.
To be eligible for this study, participants need to be at least 18 years old and have moderate to severe urinary symptoms, as determined by a specific scoring system. They should also have a prostate size of at least 30 milliliters. Participants will be monitored for safety and effectiveness of the treatment, and they will be asked to report on their urinary symptoms and overall well-being. It's important to note that individuals with certain conditions, such as prostate cancer or previous prostate surgeries, will not be able to join the study.
Gender
MALE
Eligibility criteria
- Inclusion Criteria:
- • Age ≥18 years;
- • Prostate volume ≥ 30 mL;
- • Moderate-to-severe LUTS according to International Prostatic Symptoms Score (IPSS ≥8)
- • Consent to participate;
- Exclusion Criteria:
- • Absence of consent;
- • Subsequent withdrawal of consent;
- • Diagnosis or suspicion of prostate cancer at multiparametric magnetic resonance
- • Documented bladder impaired contractility
- • Urethral stenosis
- • Previous prostate surgery
About University Of Florence
The University of Florence is a leading academic institution in Italy, renowned for its commitment to advancing scientific research and education in the medical field. With a rich history of innovation and collaboration, the university actively engages in clinical trials aimed at improving healthcare outcomes. Its multidisciplinary approach integrates cutting-edge research with clinical practice, fostering an environment that encourages the development of new therapies and treatment protocols. The University of Florence is dedicated to enhancing patient care through rigorous scientific inquiry and ethical standards in clinical research.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Florence, , Italy
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported