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Prostatic Hyperplasia clinical trials

View clinical trials related to Prostatic Hyperplasia.

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NCT ID: NCT00472251 Completed - Clinical trials for Benign Prostatic Hyperplasia

One-year Prospective Observational Study of BMI Change Effect of 5-alpha Reductase Inhibitor in Korean BPH Patients

Start date: May 2006
Phase: N/A
Study type: Observational

It is widely-accepted that serum testosterone level and BMI (body mass index) representative of the degree of obesity has negative correlation. Considering the fact that obesity is being mentioned as a risk factor for development of prostate cancer as well as other various life-threatening diseases (example: cardiovascular problems), the effect of BPH treatment agents on BMI is a subject that should certainly be elucidated. Meanwhile, to our knowledge, no prospective study has so far been performed on such issue in Asian population. Prior to generating hypothesis of the effect of 5 alpha reductase inhibitor on BMI, the real effect of 5 alpha reductase inhibitor on BMI change in Korean BPH patients has to be observed in real clinical practice. This study will test the effects of one-year medication of 5 alpha reductase inhibitor on BMI among Korean men with BPH.

NCT ID: NCT00468026 Not yet recruiting - Clinical trials for Benign Prostatic Hyperplasia

Evaluation of the ProstaPlant Prostate Stent Insertion in Ex Vivo Human Prostate

Start date: n/a
Phase: Phase 1
Study type: Interventional

The purpose of this ex-vivo study is to evaluate the insertion procedure for the ProstaPlant implant in human prostates and the support that it supplies to the prostate.

NCT ID: NCT00465101 Completed - Clinical trials for Benign Prostatic Hyperplasia

A Long-Term Study Examining the Treatment of Benign Prostatic Hyperplasia With Photoselective Vaporization

PVP
Start date: May 2007
Phase: Phase 4
Study type: Interventional

To gain clinical experience with the GreenLight HPS System, a system designed to vaporize and coagulate tissue in the treatment of benign prostatic hyperplasia to reduce lower urinary tract symptoms.

NCT ID: NCT00461123 Completed - Clinical trials for Prostatic Hypertrophy, Benign

Vardenafil in Greenlight(TM) Laser Surgery of Benign Prostate Hypertrophy

Start date: March 2007
Phase: Phase 2
Study type: Interventional

The greenlight laser has an absorption maximum which is exactly the same as for hemoglobin. In the presence of hemoglobin, its application causes vaporization of the tissue and this effect depends on the concentration of hemoglobin in the respective tissue. Therefore, increase of blood-flow in the tissue (here: prostate gland) should exert better efficacy of the laser application and consequently shortening of the required duration of laser application.

NCT ID: NCT00457457 Completed - Clinical trials for Prostatic Hyperplasia

Study the Effects of Different Doses of UK-369,003 in Men With Lower Urinary Tract Symptoms.

Start date: May 2007
Phase: Phase 2
Study type: Interventional

This is a 12 week study in which different doses and formulations of UK-369,003 will be administered to patients with a diagnosis of enlarged prostate. Patients will complete a series of questionnaires before, during and after treatment to assess if UK-369,003 has improved their urinary symptoms and erectile function . There will be several blood samples taken during the study to asses the level of drug in the blood and correlate it with the responses to the questionnaires.

NCT ID: NCT00454402 Terminated - Clinical trials for Prostatic Hyperplasia

ALF-STONE: Alfuzosin in Uretheric Stones

Start date: August 2006
Phase: Phase 3
Study type: Interventional

The aim of the study is to assess the effect of Alfuzosin compared with placebo, for 7 days, on the outcome of patients with uretheric stones submitted to Extracorporeal Shock Wave Lithotripsy (ESWL), namely in the percentage of patients without imagiologic evidence of any stone after 72h to 96 hours. This study will also specifically focus on the evaluation of time of stone clearance and of pain reduction (Numeric Rating Scale).

NCT ID: NCT00451191 Completed - Clinical trials for Benign Prostatic Hyperplasia

Botulinum Toxin Injection for the Management of BPH

MIST2
Start date: October 2006
Phase: Phase 2
Study type: Interventional

This is a double-blind randomized phase II trial to determine whether two different doses of BoNT/A injection into the prostate gland demonstrate sufficient improvement in the management of lower urinary symptoms due to BPH to warrant more extensive research. Subjects will receive either a 100U or 300U dose. Participation will last 1 year.

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).

NCT ID: NCT00435448 Terminated - Clinical trials for Benign Prostatic Hyperplasia

Study of the Efficacy and Safety of Lonidamine for the Treatment of Symptomatic Benign Prostatic Hyperplasia

Start date: June 2005
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the efficacy of lonidamine (50mg, 150mg) compared to placebo in subjects with symptomatic BPH.

NCT ID: NCT00431626 Terminated - Clinical trials for Benign Prostatic Hyperplasia

A Clinical Trial Comparing Laser TURP With and Without Dutasteride.

Start date: October 2006
Phase: Phase 3
Study type: Interventional

The purpose of this research study is to determine if the study drug Dutasteride taken before and after Laser TURP(Transurethral Resection of the Prostate), can provide effective and safe, long term improvement of lower urinary tract symptoms.