RELIEF II Study – A Prospective, Non-Randomised Multi-Centre Clinical Investigation of the Safety and Performance of GT Urological, LLC’s Phenix Device Artificial Urinary Sphincter. Investigator. Reference: UOW HREC Number: CT14/001. 2016 Clinical Trial of a new Artificial Urinary Sphincter.
Predicting risk of post-transrectal ultrasound prostate biopsy sepsis by categorising antibiotic resistance in bowel flora pre-transrectal ultrasound biopsy. Investigator. UOW HREC Number: HE13/217. The aim of this study is to investigate whether antibiotic resistant bowel flora cause a higher incidence of sepsis post-biopsy and whether a change in clinical practice and guidelines is indicated. Period: 2013 ongoing.
Safety and Feasibility of a Transurethral Endoscopic Procedure for the Luminal Restoration of the Prostatic Urethra: A Preliminary Investigation. Chief Investigator. Reference: UOW HREC Number: CT05/027. This is the first in human study for the Urolift device and is ongoing. Period: 2004 ongoing.
The LIFT Pivotal Study – Luminal Improvement Following Prostatic Tissue Approximation for the Treatment of Lower Urinary Tract Symptoms. Investigator. Reference: UOW HREC Number: CT10/09. Period: 2011 ongoing. This is a FDA approved randomised blinded multi-centre Phase 3 Pivotal trial. Recruitment is complete, and long term data is being monitored.