To Evaluate LUTS and Complications Between Indwelling Catheter and Temporary Prostatic Stent in Patients Undergoing Minimally Invasive Procedures for the Treatment of Localized Prostate Cancer or Benign Prostatic Hyperplasia (HERMES)

  • 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

info icon Willing and able to provide written informed consent prior to enrollment (if applicable).

info icon Subjects must meet all inclusion criteria to be eligible for study enrollment.

info icon Men between 18 and 85 years old.

info icon Undergo focal therapy for prostate cancer, water vapour energy ablation Rezum® or EchoLaser®.

info icon Willing to be seen by the investigator and answer questions and fill out questionnaires up to a month after surgery.

info icon Minimum age: 18

info icon Urethral stricture \<22F.

info icon Gross haematuria

info icon Prostate volume \> 80cc

info icon Prostate craniocaudal length \> 6cm

info icon Patients with long-term urinary catheters or other urinary drainage systems

info icon 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

NCT05851521

Clinic Location Investigator Distance RECRUITING STATUS Contact