Transurethral Prostate Resection (TURP) vs. Prostate Artery Embolization (PAE)
Condition(s) studied
Investigational drug(s) / intervention(s)
Prostate Artery Embolization: Prostate Artery Embolization (PAE) is performed by experienced interventional radiologists. The method involves catheterization of the prostate vessels superselectively with two to three French microcatheters. PAE is performed with microspheres of 250 to 400 µm in size.
Transurethral Prostate Resection (TURP): Under general/regional anesthesia, a resectoscope is inserted into the urethra that carries an electric metal loop (monopolar or bipolar diathermy) that is used to cut and extract the prostate tissue.
Study summary
This study focuses on the treatment of benign prostatic hyperplasia which causes lower urinary tract symptoms.
The purpose of the research project is to evaluate PAE in terms of both medical and health economic outcomes. To evaluate whether there are any differences in effect (IPSS), complications, costs and perceived quality of life compared with TUR-P.
Eligibility
Primary outcome measure(s)
- Improvement of lower urinary tract symptoms — 24 months
Assess the change in the lower urinary tract symptoms using the International Prostate Symptom Score (IPSS) questionnaire before and after prostate artery embolization procedure (PAE) compared to transurethral resection of the prostate (TURP) - Health care costs — 24 months
Assess the health care costs after prostate artery embolization procedure (PAE) compared to transurethral resection of the prostate (TURP)
Trial sites (4)
| Facility | City | Region | Status |
|---|---|---|---|
| Helsingborgs Hospital | Helsingborg | Region Skånes | Not Yet Recruiting |
| Mälarsjukhuset | Eskilstuna | Region Sörmland | Not Yet Recruiting |
| Lasarettet i Enköping | Enköping | Region Uppsala | Not Yet Recruiting |
| Region Vastmanland Hospital | Västerås | Västmanland County | Recruiting |
More Uppsala University trials in Sweden
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT05531240 on ClinicalTrials.gov ↗ ← All trials in Sweden