About this trial
Rezūm is a minimally invasive procedure that uses water vapor (steam) to treat urinary symptoms caused by an enlarged prostate (benign prostatic hyperplasia, BPH). It has been used in clinical practice since receiving FDA approval in 2015 and is recommended as a treatment option for men with moderate-to-severe urinary symptoms, including those who wish to preserve ejaculatory function. Clinical trials have shown that Rezūm improves urinary symptoms and flow rates, with benefits that last for at least five years, a low reoperation rate, and a low risk of sexual side effects.
Despite this evidence, several important questions remain. It is not well understood which patients are more likely to experience temporary urinary retention after the procedure, need repeat treatment, or develop ejaculatory changes. Standardized criteria for defining overall treatment success are also lacking.
The MISTER study is a multicenter registry designed to evaluate real-world outcomes of Rezūm therapy in patients treated in the Russian Federation. Using data from a large patient cohort, the study aims to identify factors associated with urinary retention after catheter removal, the need for repeat treatment or return to medication, and changes in ejaculatory function. The study will also develop and test combined criteria for defining treatment success.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Lower urinary tract symptoms (IPSS ≥8 points; QoL ≥3 points) due to BPH
Prostate volume of 30-150 cm³
Qmax ≤15 mL/s; post-void residual urine volume <300 mL
Prostate cancer
Disqualifiers
Patient refusal to allow use of medical data for scientific analysis
Missing or lost data required for analysis
Trial design
Single group
Treatments tested in this trial
Rezūm
Procedure/SurgeryRezūm therapy is performed transurethrally by specialists at the study centers in accordance with established clinical practice. The type of anesthesia, the number and location of water vapor injections, treatment of the median lobe, characteristics of the indwelling catheter, and duration of catheterization were determined by the attending physician.
Treatment groups
Trial outcomes
Primary outcomes
Rate of Rezūm therapy failure
Rate of Rezūm therapy failure within 12 months after the intervention, defined as the occurrence of at least one of the following events: * Resumption or continuation of medical therapy for LUTS/BPH * Repeat surgical intervention for BPH * Failure to restore voiding
Secondary outcomes
Post-void residual urine volume
14 days
International Prostate Symptom Score (IPSS)
Mild LUTS (symptom score less than of equal to 7) Moderate LUTS (symptom score range 8-19) Severe LUTS (symptom score range 20-35)
Qmax
Prostate volume
Sponsors and contacts
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Sechenov University
Lead sponsor
Russian University of Medicine
Collaborator
N. I. Pirogov Clinic of High Medical Technologies
Collaborator
UGMK-Zdorovie Medical Center
Collaborator
SM-Clinic Multidisciplinary Medical Holding
Collaborator
MEDSI Group of Companies
Collaborator
URO-PRO Clinic
Collaborator
Avicenna Clinical Hospital
Collaborator
Neftyanik Medical and Sanitary Unit
Collaborator
St. Luke's Clinical Hospital
Collaborator
N. A. Semashko Railway Clinical Hospital ("RZD-Meditsina")
Collaborator
Liniya Zhizni LLC
Collaborator
S. P. Botkin Moscow Multidisciplinary Scientific and Clinical Center
Collaborator
European Medical Center
Collaborator
RTH (Real Trans Hair) Medical Center
Collaborator