Optimized Water Vapor Thermal Therapy for Benign Prostatic Hyperplasia
1 other identifier
interventional
58
0 countries
N/A
Brief Summary
Water vapor thermal therapy (Rezum) is a minimally invasive treatment for benign prostatic hyperplasia (BPH) that uses injections of sterile water vapor directly into the prostate for tissue ablation.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Sep 2024
Typical duration for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 1, 2024
CompletedFirst Submitted
Initial submission to the registry
September 5, 2024
CompletedFirst Posted
Study publicly available on registry
September 23, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
September 1, 2027
ExpectedSeptember 23, 2024
September 1, 2024
1 year
September 5, 2024
September 20, 2024
Conditions
Outcome Measures
Primary Outcomes (1)
International Prostate Symptom Score (IPSS) change from baseline to 3 months.
International prostate symptom score (IPSS) is a questionnaire used to indicate the severity of LUTS symptoms, There are 7 questions relating to different symptoms subjects be experiencing. 7 questions about patients' urinating include Incomplete emptying, Frequency, Intermittency, Urgency, Weak stream, Straining and Nocturia, every question have 0-5 scores according to Prostate Symptom, the higher score mean patient have more severe the symptoms. IPSS total score: the minimum score is 0 and maximum score are 35. IPSS total 0-7 scores are mild symptoms, IPSS total 8-19 scores are moderate symptoms and IPSS total 20-35 scores are severe symptoms. International Prostate Symptom Score (IPSS) scores were recorded at baseline to 3 months. The mean change in IPSS was calculated.
3 months
Secondary Outcomes (6)
International Prostate Symptom Score (IPSS) change from baseline to 1 month, 3 months, 6 months, 1 year, then annually to 3 years.
1 month, 3 months, 6 months, 1 year, then annually to 3 years
The change of peak flow rate (Qmax)
1 month, 3 months, 6 months, 1 year, then annually to 3 years
Post void residual urine volume (PVR)
1 month, 3 months, 6 months, 1 year, then annually to 3 years
Quality of life (QoL) questionnaire
1 month, 3 months, 6 months, 1 year, then annually to 3 years
Ejective function (MSHQ-EjD)
1 month, 3 months, 6 months, 1 year, then annually to 3 years
- +1 more secondary outcomes
Study Arms (1)
Optimized Water Vapor Thermal Therapy
EXPERIMENTALThe Rezum System is designed to treat patients with urinary symptoms associated with BPH.
Interventions
The Rezum System is designed to treat patients with urinary symptoms associated with BPH. The Rezum System utilizes radiofrequency current to generate thermal energy in the form of water vapor, which is then injected into the transition zone and/or median lobe of the prostate in controlled 9-second doses. The vapor injected into the prostate tissue rapidly disperses through the interstitial space between the tissue cells. As the vapor cools, it condenses immediately on contact with tissue, and the stored thermal energy is released, denaturing the cell membranes and causing cell death.
Eligibility Criteria
You may qualify if:
- Male subjects ≥ 45 years of age who have obstructive symptoms secondary to BPH requiring invasive intervention.
- IPSS score of ≥ 13.
- Qmax: Peak flow rate ≤ 15 ml/sec.
- Post-void residual (PVR) \< 300 ml.
- Prostate volume \> 30 ml.
- Subject able to complete the study protocol in the opinion of the Principal Investigator.
You may not qualify if:
- History of any illness or surgery that in the opinion of the Principal Investigator may confound the results of the study.
- Any prior minimally invasive intervention or surgical intervention for the symptoms of BPH.
- Currently enrolled in another clinical trial.
- Confirmed or suspected malignancy of prostate or bladder.
- Documented active urinary tract infection by culture or bacterial prostatitis.
- Neurogenic bladder or sphincter abnormalities.
- Urethral strictures, bladder neck contracture or muscle spasms.
- Subjects who are interested in maintaining fertility.
- Significant urge incontinence.
- Unable or unwilling to sign the Informed Consent Form.
- Any cognitive disorder that interferes with or precludes a subject from directly and accurately communicating with the Principal Investigator regarding the study.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 5, 2024
First Posted
September 23, 2024
Study Start
September 1, 2024
Primary Completion
September 1, 2025
Study Completion (Estimated)
September 1, 2027
Last Updated
September 23, 2024
Record last verified: 2024-09