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HIFU for Benign prostatic hyperplasia

High-Intensity Focused ultrasound for Benign prostatic hyperplasia

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CRIS
Registry ID
KCT0003780
Enrollment
10
Registered
2019-04-15
Start date
2019-03-25
Completion date
Unknown
Last updated
2019-04-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Patients with benign prostate hyperplasia that meet the criteria for selection / exclusion should be admitted on the day of admission, followed by general anesthesia Only one procedure is performed (e

Sponsors

The Catholic University of Korea, Seoul St. Mary's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: - Over 50 years old - prostate volume <80 cm3 - peak Qmax <15 ml / s - postvoid residual (PVR) volume <300 cc - International Prostate Symptom Score (IPSS) > 12

Exclusion criteria

Exclusion criteria: - If transrectal ultrasonography is not possible. - rectum - if you have an active disease of the anus - If you have undergone pseudoradicular prostate surgery within 2 months - If anesthesia is not appropriate - If there is severe calcification (> 1 cm) that can not be done with focused ultrasound treatment (except when the calcification is removed by performing pseudo-prosthetic surgery before 2 months of focused ultrasound) - If there is a metal stent in the urethra - If you have a problem with hemostasis

Design outcomes

Primary

MeasureTime frame
International Prostate Symptom Score (IPSS)

Secondary

MeasureTime frame
Postvoid residual (PVR);Prostate volume

Countries

Korea, Republic of

Contacts

Public ContactKyu Won Lee

The Catholic University of Korea, Seoul St. Mary's Hospital

firss@hanmail.net+82-2-2258-6366

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026