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Benign Prostatic Hypertrophy clinical trials

View clinical trials related to Benign Prostatic Hypertrophy.

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NCT ID: NCT04398420 Terminated - Clinical trials for Benign Prostatic Hypertrophy

Transurethral Vapor Enucleation Resection of the Prostate (TVERP), Bipolar TURis and HoLEP

Start date: August 27, 2020
Phase: N/A
Study type: Interventional

To verify the safety and efficacy of the use of the plasma vaporisation button in Transurethral Vapor Enucleation and Resection of the prostate (TVERP) for treatment of Benign prostatic hypertrophy (BPH) patients with prostate ˃30 and ≤80 ml compare to TURis or HoLEP surgery methods.

NCT ID: NCT02676544 Terminated - Clinical trials for Lower Urinary Tract Symptoms

Prostate Embolization for Massive Benign Prostatic Hypertrophy (BPH)

Start date: December 2015
Phase: Phase 1/Phase 2
Study type: Interventional

This is a prospective, open label single center feasibility study to demonstrate basic safety and effectiveness of prostate artery embolization for the treatment of symptomatic benign prostatic Hyperplasia (BPH) in a small series of patients with large (≥90 grams) glands.

NCT ID: NCT00449150 Terminated - Clinical trials for Benign Prostatic Hypertrophy

Cetrorelix (CET) Pamoate Regimens in Patients With Symptomatic Benign Prostatic Hypertrophy (BPH)

Start date: March 2007
Phase: Phase 3
Study type: Interventional

Benign Prostatic Hypertrophy (BPH) is a common and bothersome condition of aging men. It is characterized by an enlargement of the prostate occurring in human male over the age of 50 which increases in prevalence with age, and among those aged 50 to 80, about 40% report moderate or severe urinary symptoms of prostatism. The aim of treatment is to improve patients' quality of life which primarily depends on the severity of the symptoms of BPH. Current treatments of BPH have a benefit / risk ratio which leaves room for improvement. For this study, study medication (Cetrorelix pamoate or placebo) is administered by injection in the buttocks (Intramuscular). All patients completing the double-blind portion (Week 0 to 52) are eligible to receive the active drug during the open-label part of the study (Week 52 to 90).