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Prostatic Hyperplasia clinical trials

View clinical trials related to Prostatic Hyperplasia.

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NCT ID: NCT01637701 Completed - Clinical trials for BPH With Large Prostate

Plasmakinetic Enucleation of the Prostate to Treat Benign Prostatic Hypertrophy Patients With Large Prostate

Start date: June 2004
Phase: N/A
Study type: Interventional

The goal of this study is to compare the perioperative and postoperative characters of plasmakinetic enucleation of the prostate(PkEP) with bipolar TURP(B-TURP) for BPH patients with large prostate.

NCT ID: NCT01627522 Completed - Clinical trials for Benign Prostate Hyperplasia

Evaluation of Finastride Effect in Different Dosage on the Amount of Perioperative Bleeding in Transurthral Resection of Prostate

TURP
Start date: January 2012
Phase: Phase 2/Phase 3
Study type: Interventional

Preoperative use of finastride will decrease the amount of perioperative blood loss during and after TURP The effect of finastride on decreasing the amount of perioperative blood loss during and after TURP is dose dependent Finastride will decrease microvascular density in prostate tissue and this effect is dose dependent

NCT ID: NCT01604811 Completed - Clinical trials for Benign Prostatic Hyperplasia (BPH)

Exploratory Study of L.S.E.S.r. (LipidoSterolic Extract of Serenoa Repens)(PERMIXON® 160 mg Hard Capsule) Versus Tamsulosine LP Activity on Inflammation Biomarkers in Urinary Symptoms Related to BPH (Benign Prostatic Hyperplasia)

PERMIN
Start date: June 2012
Phase: Phase 4
Study type: Interventional

Inflammation is reported as one of the most recent hypotheses to explain BPH. Recent published works pointed out that urine and serum markers could be used for detection of prostatic inflammation. The aim of the study is to assess the activity on inflammation biomarkers (serum and urine inflammation markers) of Permixon® 160 mg hard capsule and Tamsulosine Arrow LP in the treatment of urinary symptoms related to BPH. The potential links between serum and urinary markers of inflammation and BPH clinical symptoms at baseline and on treatment will be explored.

NCT ID: NCT01604148 Completed - Clinical trials for Benign Prostatic Hyperplasia

Retrospective Review a Comprehensive Case Database of HoLEP Procedure Performed by a Single Surgeon

Start date: July 2011
Phase: N/A
Study type: Observational

Persistent detrusor overactivity (DO) after transurethral prostatectomy results in symptomatic failure in more than one third of the patients. Storage symptoms are major complaints in the early postoperative period after Holmium Laser Enucleation of the Prostate (HoLEP). To investigate the effect of DO in the patients with Benign Prostatic Obstruction (BPO), the investigators evaluated the changes in the storage symptoms following HoLEP in conjunction with the prescription of the anticholinergic drugs.

NCT ID: NCT01589263 Completed - Clinical trials for Benign Prostatic Hyperplasia

Effectiveness of onaBoNT-A vs Oral Tamsulosin in Men With BPH and LUTS

Start date: June 1, 2012
Phase: Phase 2
Study type: Interventional

Benign prostatic hyperplasia (BPH) and its related symptoms are a common condition that affects nearly half of men over age 50 and 90% of men over 80. Lower urinary tract symptoms (LUTS) caused by BPH can be very troublesome, affect an individual's quality of life significantly, and are costly. his Phase 2 clinical research trial is a double-blind, randomized, placebo-controlled, parallel-group study to compare the treatment effects of onaBoNT-A 200 U versus 0.4 mg per day of oral tamsulosin in male Veterans diagnosed with moderate to severe LUTS [American Urologic Association Symptom Score (AUASS) equal to or greater than 8] associated with BPH. A total of 74 volunteers will be recruited to participate in this clinical trial. Volunteers will include only males who are greater than 50 years of age and diagnosed with LUTS associated with BPH. They are Veterans who visit the Michael E. DeBakey Veterans Affairs Medical Center - Houston (MEDVAMC). There are no eligibility restrictions as to race or ethnicity.

NCT ID: NCT01577693 Completed - Clinical trials for Prostatic Hyperplasia

Study to Compare the Bioavailability of Dutasteride Novel Formulation Form to the Soft Gel Capsule Form in Healthy Male Subjects

ARI115148
Start date: May 12, 2011
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the bioavailability of 0.5mg dutasteride novel formulation compared to the currently marketed 0.5mg dutasteride soft gel capsule in fasted healthy male subjects.

NCT ID: NCT01566292 Completed - Clinical trials for Benign Prostatic Hyperplasia (BPH)

Intraprostatic Botulinum Toxin Type "A" Injection in Patients With Benign Prostatic Hyperplasia and Unsatisfactory Response to Medical Therapy

Start date: September 2009
Phase: Phase 2/Phase 3
Study type: Interventional

The injection of botulinum neurotoxin A into the prostate represents an alternative, minimal invasive treatment in patient with lower urinary tract symptoms (LUTS) associated to benign prostatic hyperplasia (BPH). Objective: To evaluate the effectiveness of BTA in treating patients with symptomatic BPH and unsatisfactory response to combined medical therapy.

NCT ID: NCT01534793 Completed - Clinical trials for Benign Prostatic Hyperplasia

QUAPELLA (QUAlity of Prostate Enucleation by LUMENIS - Laser)

QUAPELLA
Start date: February 2012
Phase: N/A
Study type: Observational

This observational study aims at describing the learning curve of the Holmium Enucleation of the Prostate (HoLEP) technique using a LUMENIS laser device by senior attending urologists.

NCT ID: NCT01534351 Terminated - Clinical trials for Benign Prostatic Hyperplasia

Comparison of Finasteride and Tamsulosin for Treatment of Benign Prostatic Hyperplasia (BPH) (MK-0906A-149 AM2)

Start date: August 1, 2013
Phase: Phase 3
Study type: Interventional

This study is designed to compare safety and efficacy of monotherapy finasteride to combination therapy (finasteride and tamsulosin) in Asian men with benign prostatic hyperplasia (BPH) who are at least 50 years of age or older. The primary hypotheses are that concomitantly-dosed finasteride 5 mg and tamsulosin 0.2 mg will be superior with respect to BPH symptoms compared to monotherapy with finasteride 5 mg as measured by change from baseline on the International Prostate Symptoms Score (IPSS) and will be superior with respect to prostate volume reduction compared to montherapy with tamsulosin 0.2 mg as measured by percent change from baseline in prostate volume.

NCT ID: NCT01533038 Completed - Clinical trials for Benign Prostatic Hyperplasia

BPH-6: Comparison of the UroLift System to TURP for Benign Prostatic Hyperplasia

BPH-6
Start date: February 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the UroLift System Treatment to Transurethral Resection of the Prostate (TURP) in improving a patient's overall quality of life, while evaluating healthcare expenditures associated with each therapy.