drugset / Trial / NCT04446598

Management of Prostatodynia in Younger Patients With Non-ablative Erbium:YAG Intraurethral Laser

NCT04446598

Completed 36 enrolled Adrian Gaspar
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This prospective study aimed to compare the clinical outcomes between the use of the erbium: YAG (Er:YAG) laser, intraurethrally administered in long non-ablative SMOOTH™ train of pulses applied at the level of the male prostatic urethra, to the use of the pharmacological treatment of oral tadalafil for the treatment of chronic prostatitis/chronic pelvic pain syndrome (CP/CPPS). The results show that both treatments are effective in alleviating symptoms of CP/CPPS. The non-ablative Er:YAG SMOOTHTM laser seems to be a promising treatment for this widely spread condition. More studies are needed to confirm its safety and efficacy.

Timeline

Start
2017-03-13
Primary completion
2018-11-30
Completion
2018-12-31

Drugs

EvaluationDrugModalityDoseRoute
Comparator Tadalafil Small molecule 5 mg Oral

Indications