Clinical Trials Logo

Hyperplasia clinical trials

View clinical trials related to Hyperplasia.

Filter by:

NCT ID: NCT00386009 Completed - Clinical trials for Benign Prostatic Hyperplasia

Effects of Tadalafil Once a Day for 12 Weeks in Men With Signs and Symptoms of Benign Prostatic Hyperplasia

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

The purpose of this study is to evaluate the function of the bladder and urethra during urinary storage or voiding in men with signs and symptoms of benign prostatic hyperplasia treated with either placebo or tadalafil.

NCT ID: NCT00384930 Completed - Clinical trials for Benign Prostatic Hyperplasia

Study of Tadalafil Once-a Day for 12 Weeks in Men With Signs and Symptoms of Benign Prostatic Hyperplasia

Start date: August 2006
Phase: Phase 2/Phase 3
Study type: Interventional

This is a randomized, double-blind, placebo-controlled, parallel-design, multinational, 12-week study to compare the efficacy, dose response, and safety of tadalafil once a day versus placebo in men with signs and symptoms of benign prostatic hyperplasia, including lower urinary tract symptoms.

NCT ID: NCT00381108 Unknown status - Clinical trials for Benign Prostatic Hyperplasia

Study of the Effects of Pomegranate Tablets on Enlarged Prostates

Start date: September 2005
Phase: Phase 1
Study type: Interventional

To determine whether pomegranate tablets have a therapeutic effect on Benign Prostatic Hyperplasia.

NCT ID: NCT00379366 Terminated - Thrombosis Clinical Trials

External Ionizing Radiation to Prevent Restenosis on Haemodialysis Vascular Access

RASTA
Start date: December 2006
Phase: Phase 2/Phase 3
Study type: Interventional

Although ionizing radiations have been proposed for the prevention of intimal hyperplasia in coronary and peripheral arteries, information is lacking on how irradiation may prevent neointimal smooth-muscle cell proliferation and restenosis on prosthetic haemodialysis vascular access. We will assess the preventive effect of one dose of radiations (14 Gy) administered transcutaneously one day after dilatation of stenosis on prosthetic haemodialysis vascular access in a randomized controlled trial with a standardized clinical and ultrasonographic one-year follow-up.

NCT ID: NCT00379067 Completed - Clinical trials for Benign Prostatic Hyperplasia

A Phase 4 Study With Tamsulosin OCAS to Assess Nighttime Voiding.

Start date: October 2005
Phase: Phase 4
Study type: Interventional

Randomized, double-blind, placebo-controlled study with two treatment arms (Tamsulosin OCAS 0.4 mg & placebo). The study comprises a 2-week placebo run-in followed by a 12-week treatment period.

NCT ID: NCT00375765 Completed - Prostate Cancer Clinical Trials

Effects On Dihydrotestosterone Regulated Gene Expression In Benign Prostatic Hyperplasia Or Prostate Cancer

Start date: April 2005
Phase: Phase 4
Study type: Interventional

Dutasteride is used in the treatment of benign prostate enlargement (BPH).It inhibits conversion of testosterone (T) into the more potent dihydrotestosterone (DHT) to stop prostate (and possibly prostate cancer) growth. DHT regulates the expression of certain genes in the prostate. The pharmacodynamics of DHT reduction in the prostate were never investigated until now, as every measurement would require prostate tissue retrieval, which is medically and ethically unacceptable. A recently developed test is able to quantitatively measure gene expression in prostate-borne cells, in urine sediments after prostate massage. By measuring this gene expression in patients using dutasteride, it has become possible to assess the pharmacodynamics of gene expression reduction, which is representative for the pharmacodynamics of DHT reduction. Repeated prostate tissue sampling has therefore become unnecessary. This newly gained knowledge will lead to a better understanding of the action of dutasteride and will possibly help improve treatment of symptomatic BPH (Benign Prostatic Hyperplasia) and PrCa (Prostate Cancer)in the future.

NCT ID: NCT00368979 Completed - Clinical trials for Prostatic Hyperplasia

Dutasteride (GI198745) In Benign Prostatic Hyperplasia Subjects

Start date: February 17, 2006
Phase: Phase 3
Study type: Interventional

This study will assess the efficacy and safety of GI198745 0.5mg given once daily for 52 weeks to Benign Prostatic Hyperplasia (BPH) patients.

NCT ID: NCT00364585 Completed - Clinical trials for Benign Prostatic Hyperplasia

A Prospective Evaluation of the GreenLight Model 120 Laser

Start date: May 2006
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the performance of the GreenLight™ model 120 delivering higher average power to allow for more flexibility in the working distance of the delivery device with the same power density to tissue as that of the current GreenLight model. In addition this study will examine the Laserscope GDD (guided delivery device) that has been designed exclusively for use with the GreenLight™ model 120.

NCT ID: NCT00361933 Withdrawn - Clinical trials for Giant Lymph Node Hyperplasia

Valganciclovir to Treat HHV-8 Associated Multicentric Castleman's Disease

Start date: December 2008
Phase: Phase 4
Study type: Interventional

The purpose of the study is to learn whether people who are experiencing an MCD (multicentric Castleman's Disease) flare will improve after taking valganciclovir. MCD is a type of inflammatory disease associated with Human Herpesvirus 8 (HHV-8). Valganciclovir is FDA approved for treating a different type of Human Herpesvirus, but not approved for the treatment of HHV-8. It is therefore considered experimental in this study.

NCT ID: NCT00359905 Completed - Clinical trials for Benign Prostatic Hyperplasia

Evaluation of the Efficacy and Safety of Silodosin in the Treatment of the Signs and Symptoms of BPH

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

A new drug for the treatment of benign prostatic hyperplasia is compared with placebo and tamsulosin (a drug belonging to the same therapeutic class) for to determine if it is safe and effective (the first phase of the study lasts approximately 18 weeks) and then is used for another 9 months to determine its long-term safety.