- Not Yet Recruiting
- Treatment
- Interventional
- Randomized
- Device
- Lyx Institute
- 18 - 85 Years
Study Purpose
The goal of this single-centre prospective randomized clinical trial is to compare the post-operative use of temporary prostatic stent (Group 1) vs indwelling catheter (Group 2) in patients undergoing cryotherapy for targeted therapy of localized prostate cancer, transurethral water vapor energy ablation (REZUM) or transperineal laser ablation of the prostate with EchoLaser™ system for the treatment of benign prostatic hyperplasia (BPH) The main questions are: * Difference in quality of life, Lower Urinary Tract Symptoms (scored with IPSS, International Prostate Symptom Score), urinary continence symptoms (scored with International Consultation on Incontinence Questionnaire-Urinary Incontinence Short Form, ICIQ-UI-SF) and patient satisfaction between indwelling catheter and temporary prostatic stent (Exime®) score with a non-validated questionnaire (Stent/catheter-related urinary symptoms questionnaire) * Difference in side effects and complications between indwelling catheter and temporary prostatic stent (Exime®) A total 120 of patients will be enrolled (Group 1: 60; Group 2: 60) with a 1:1 randomization ratio. The follow-up duration will be 6 months.
Intervention
Device : Temporary prostatic stent (Exime®)
Device : Indwelling catheter
Eligibility Requirements
Willing and able to provide written informed consent prior to enrollment (if applicable).
Subjects must meet all inclusion criteria to be eligible for study enrollment.
Men between 18 and 85 years old.
Undergo focal therapy for prostate cancer, water vapour energy ablation Rezum® or EchoLaser®.
Willing to be seen by the investigator and answer questions and fill out questionnaires up to a month after surgery.
Minimum age: 18
Urethral stricture \<22F.
Gross haematuria
Prostate volume \> 80cc
Prostate craniocaudal length \> 6cm
Patients with long-term urinary catheters or other urinary drainage systems
Lack of commitment on the part of the patient to attend the follow-up as required.
Recruiting status
Not Yet Recruiting
Estimated enrollment
120
Study start date
Jun 30, 2023
Study end date
Jun 30, 2025
Last updated
Mar 23, 2025
Primary purpose
Treatment
Design
Interventional
Intervention
Device
Study phase
NA
Allocation
Randomized
Sponsor:
Lyx Institute
Collaborator:
N/A
Investigator:
Juan I Martinez-Salamanca, MD PhD FEBU FACS FEBSM
Publications
Websites
N/A
NCT05851521
Clinic | Location | Investigator | Distance | RECRUITING STATUS | Contact |
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