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Clinical Trial Summary

This registry study aims to collect data on efficacy and safety of different treatments of benign prostatic enlargement (BPE) and lower urinary tract symptoms associated with benign prostatic hyperplasia (BPH-LUTS).


Clinical Trial Description

This registry study aims to collect data on efficacy and safety of different treatments of benign prostatic enlargement (BPE) and lower urinary tract symptoms associated with benign prostatic hyperplasia (BPH-LUTS). Clinical, patient reported and imaging data that are assessed in clinical routine will be prospectively collected. All patients that are treated for BPE / BPH-LUTS at our institution will be included if they provide written informed consent. This registry enables us to compare novel treatment option (e.g. prostatic artery embolization; PAE) to established interventions (e.g., TURP, HoLEP, open prostatectomy, ThuLEP, Thulium laser vaporization, TUIP) regarding safety and efficacy. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03521648
Study type Observational [Patient Registry]
Source Cantonal Hospital of St. Gallen
Contact Dominik Abt, MD
Phone +41 71 494 14 16
Email dominik.abt@kssg.ch
Status Recruiting
Phase
Start date July 7, 2017
Completion date December 1, 2027

See also
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