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Study identifier: NCT06725212 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Evaluation of the Water Vapor Thermal Therapy System for the Treatment of Benign Prostatic Hyperplasia

Condition: Benign Prostatic Hyperplasia  ·  Sponsor: Medtecx Co Ltd.

PhaseNA
Planned participants126
Who can joinMale, 45 Years to 80 Years
Healthy volunteersNo

About this study

To evaluate the efficacy and safety of the Water Vapor Thermal Therapy system for the treatment of Benign Prostatic Hyperplasia under the premise of ensuring the safety of the subjects and ensuring the scientific nature of the clinical trial. The primary safety endpoint will be device-related (serious) adverse events. The primary effectiveness endpoint will be changes (treatment group vs control group) from baseline in International Prostate Symptom Score (IPSS) 3 months after medical device intervention.

This description comes directly from the study's public registry record.

Talk to the study team

Jim Zhang, MD  ·  jim.zhang@medtecx.com  ·  jim.zhang@medtecx.com

Always discuss trial participation with your own doctor first.

Locations (10)

The First Affiliated Hospital of Anhui Medical UniversityHefei, Anhui, ChinaRecruiting
Beijing Luhe Hospital Affiliated to Capital Medical UniversityBeijing, Beijing Municipality, ChinaRecruiting
BeiJing Tsinghua Changgung HospitalBeijing, Beijing Municipality, ChinaRecruiting
PLA General HospitalBeijing, Beijing Municipality, ChinaRecruiting
Tongji Hospital Affiliated to Tongji Medical College of Huazhong University of Science and TechnologyWuhan, Hubei, ChinaRecruiting
The Second Affiliated Hospital of Nanjing Medical UniversityNanjing, Jiangsu, ChinaRecruiting
The First Affiliated Hospital of Nanchang UniversityNanchang, Jiangxi, ChinaRecruiting
The First Affiliated Hospital of Xi'an Jiaotong UniversityXi'an, Shaanxi, ChinaRecruiting
Shanghai First People's HospitalShanghai, Shanghai Municipality, ChinaRecruiting
The Second Hospital of Tianjin Medical UniversityTianjin, Tianjin Municipality, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06725212