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Lower Urinary Tract Symptoms clinical trials

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NCT ID: NCT01097707 Terminated - Clinical trials for Benign Prostatic Hyperplasia

A Study in Men With Benign Prostatic Hyperplasia

Start date: April 2010
Phase: Phase 2
Study type: Interventional

The purpose of the study is to determine whether LY500307 helps symptoms of Benign Prostatic Hyperplasia (BPH)

NCT ID: NCT01078545 Completed - Clinical trials for Lower Urinary Tract Symptoms

Lucrin® Depot Efficacy and Safety Monitoring Study in Patients With Advanced Prostate Cancer and Lower Urinary Tract Symptoms (LUTS)

LEMON
Start date: September 2008
Phase: N/A
Study type: Observational

The purpose of the study is to determine the influence of GnRH (gonadotropin releasing hormone) analogue - Lucrin Depot 11.25 mg (Lucrin Depot 3.75mg - in Ukraine) administration on intensity of lower urinary tract symptoms (LUTS) in patients with diagnosed locally advanced and/or metastatic prostate cancer and LUTS.

NCT ID: NCT01042249 Completed - Stroke Clinical Trials

Pelvic Floor Muscle Training(PFMT) on Lower Urinary Tract Symptoms (LUTS) in Men With Stroke

Start date: February 2010
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the effect of pelvic floor muscle training (PFMT) on Lower Urinary Tract Symptoms (LUTS) in men after stroke. 120 men with LUTS or increased LUTS after stroke is included and randomized into a treatment group or a control group. The subjects in the treatment group follows a 12 week standard PFMT program, while the control group is not given specific treatment of their LUTS but like the treatment group follows the standard rehabilitation program for stroke patient. Outcome are measured by - 5 questionnaires - Voiding diary - 24-hour pad test - pelvic floor muscle assessment test

NCT ID: NCT01021332 Completed - Clinical trials for Benign Prostatic Hyperplasia

Long Term Study of Solifenacin Succinate and Tamsulosin Hydrochloride Oral Controlled Absorption System (OCAS) in Males With Lower Urinary Tract Symptoms

Neptune II
Start date: April 26, 2010
Phase: Phase 3
Study type: Interventional

Clinical study to examine the safety, tolerability and efficacy of long-term combination therapy of tamsulosin and solifenacin in the treatment of males with lower urinary tract symptoms (LUTS) associated with benign prostatic hyperplasia (BPH) with a substantial storage component.

NCT ID: NCT01018511 Completed - Clinical trials for Benign Prostatic Hyperplasia

Study of Solifenacin Succinate and Tamsulosin Hydrochloride OCAS in Males With Lower Urinary Tract Symptoms

Neptune
Start date: January 2010
Phase: Phase 3
Study type: Interventional

Clinical study to examine the efficacy, safety and tolerability of combination therapy of tamsulosin hydrochloride and solifenacin succinate compared to monotherapy of tamsulosin hydrochloride in the treatment of males with LUTS associated with BPH with a substantial storage component.

NCT ID: NCT01003249 Terminated - Constipation Clinical Trials

Dysfunctional Voiding and Lower Urinary Tract Symptoms With Baclofen

Start date: September 2009
Phase: Phase 4
Study type: Interventional

Dysfunctional voiding is often associated with constipation. The association of constipation with urologic pathologic processes has previously been described since the 1950's, but it was only over the past decade that clinicians have paid more attention to this relationship and recognized it existence with the term dysfunctional elimination syndrome (DES). This term is used to reflect the broad spectrum of functional disturbances that may affect the urinary tract including that of functional bowl disturbances and can be classified as follows: - Functional disorder of filling: overactive bladder, over distention of bladder or insensate bladder, which may be associated with fecal impaction or rectal distention with infrequent bowel movements - Functional disorder of emptying: over-recruitment of pelvic floor activity during voiding causing interrupted and/or incomplete emptying also associated with defecation difficulties due to non- relaxation of the puborectalis muscle, dyssynergic defecation or pain with defecation Several different therapeutic options have been used for patients with dysfunctional voiding mainly to decrease bladder outlet obstruction. These treatments including, alpha adrenergic antagonists, and botulinum toxin are less than optimum. One possible explanation for these drug failures includes the inability of these medications to relax the striated muscles of the pelvic floor necessary for voiding. To date there has been no data to evaluate the role of baclofen on the striated muscle of the external anal sphincter, essential in the defecation process.

NCT ID: NCT01002664 Completed - Clinical trials for Benign Prostatic Hyperplasia

Efficacy and Safety of MCS-2 in the Treatment of Lower Urinary Tract Symptoms

MCS_LUTS
Start date: May 2010
Phase: Phase 3
Study type: Interventional

The hypothesis of the study is to examine whether MCS-2 is safe and effective in the treatment of lower urinary tract symptoms suggestive of benign prostatic hyperplasia.

NCT ID: NCT01002417 Completed - Clinical trials for Benign Prostatic Hyperplasia

MCS in the Treatment of Lower Urinary Tract Symptoms

MCS_LUTS
Start date: July 2010
Phase: Phase 2/Phase 3
Study type: Interventional

The hypothesis of the study is to examine whether MCS-2 is safe and effective in the treatment of lower urinary tract symptoms suggestive of benign prostatic hyperplasia.

NCT ID: NCT01002274 Completed - Clinical trials for Benign Prostatic Hyperplasia

Open-Label Extension Study of MCS-2 in the Treatment of Lower Urinary Tract Symptoms

MCS-2-TWN-c
Start date: August 2010
Phase: Phase 3
Study type: Interventional

This is an open-label extension study of another study protocol, MCS-2-TWN-a. Subjects who have completed the 12-week treatment and procedures under the protocol MCS-2-TWN-a will be eligible for this study.

NCT ID: NCT01002222 Completed - Clinical trials for Benign Prostatic Hyperplasia

Open-Label Extension Study of MCS-2 in the Treatment of Lower Urinary Tract Symptoms (MCS-2-US-c)

MCS-2-US-c
Start date: January 2011
Phase: Phase 3
Study type: Interventional

This is an open-label extension study of another study protocol, MCS-2-US-a. Subjects who have completed the 12-week treatment and procedures under the protocol MCS-2-US-a will be eligible for this study.