Clinical Trials Logo

Enuresis clinical trials

View clinical trials related to Enuresis.

Filter by:

NCT ID: NCT00547378 Completed - Overactive Bladder Clinical Trials

InSite for Over Active Bladder

InSite - OAB
Start date: October 2007
Phase: Phase 4
Study type: Interventional

The purposes of this study are: 1. To provide evidence from a randomized controlled trial that InterStim Therapy provides better relief of symptoms of OAB than standard medical treatments in current use. 2. To fulfill the requirements of the FDA-mandated post-approval study of the safety of the tined lead using a minimally invasive approach.

NCT ID: NCT00463554 Completed - Clinical trials for Stress Urinary Incontinence

TVT-SECUR A Pilot Study for the Treatment of Stress Urinary Incontinence

Start date: April 1, 2006
Phase:
Study type: Observational

The primary objective of this study is to obtain clinical performance information on the GYNECARE TVT-SECUR* System (Tension-free Support for Incontinence) in women with stress urinary incontinence (SUI).

NCT ID: NCT00392210 Completed - Clinical trials for Urinary Incontinence

Assessment of Two Postoperative Techniques Used to Predict Voiding Efficiency After Gynecologic Surgery

Start date: October 2006
Phase: N/A
Study type: Interventional

After gynecologic surgery, it may be difficult to void (urinate). This problem is usually short-term with normal function returning within a few days to a few weeks. For this reason, patients may require drainage of their bladder with a catheter immediately after surgery. Currently in our office, we use two different tests to see how well you are able to urinate and how quickly the catheter can be removed. The purpose of this study is to see which voiding test is better after gynecologic surgery.

NCT ID: NCT00321477 Completed - Overactive Bladder Clinical Trials

A Study Of GW679769 Compared To Placebo In Women With Overactive Bladder

Start date: December 2005
Phase: Phase 2
Study type: Interventional

This is a Phase IIa study to evaluate the efficacy, safety and tolerability of GW679769 vs placebo on symptoms of urgency with urge incontinence, frequency and nocturia associated with overactive bladder in women.

NCT ID: NCT00277095 Completed - Clinical trials for Urinary Incontinence

ProACT Therapy for the Treatment of Stress Urinary Incontinence in Males

ProACT
Start date: August 2005
Phase: N/A
Study type: Interventional

The purpose of the study is to evaluate the safety and effectiveness of a minimally invasive surgical procedure in up to 109 male patients. The ProACT device is designed to treat men who have stress urinary incontinence arising from intrinsic sphincter deficiency following an operation performed on the prostate for cancer or for benign prostatic hyperplasia. Two adjustable balloons (one on each side of the urethra) are implanted to treat urinary stress incontinence. The results will be analyzed to demonstrate the effects of the device as well as its associated risks. Therapeutic success will be based on whether patients demonstrate at least a 50% reduction in pad weight at 18 months follow-up compared to the pad weight results at baseline.

NCT ID: NCT00270998 Completed - Clinical trials for Urinary Incontinence

ATLAS: Ambulatory Treatments for Leakage Associated With Stress

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

Stress urinary incontinence is the uncontrollable leakage of urine with physical effort or stress, such as coughing, sneezing, or exercise. Treatment for stress incontinence can be surgical or non-surgical. Different non-surgical treatments include pelvic muscle exercises and pessary use. Pelvic muscle exercises (often known as "Kegel" exercises) train and strengthen the pelvic muscles and improve incontinence. A pessary is a medical device that fits inside the vagina to give the urethra and bladder extra support and prevent or reduce urinary incontinence. Exercises and pessary use can help women with stress incontinence but it is not known which treatment is better, or if a combination of the two treatments at the same time is best. This study will determine whether pelvic muscle training and exercises, pessary use, or a combination of both exercises and pessary is most effective at improving incontinence in women. The study's primary hypothesis is that pessary use is more effective than pelvic muscle exercises after 3 months of treatment.

NCT ID: NCT00270621 Completed - Enuresis Clinical Trials

Family Help Program: Nighttime Enuresis Treatment Program

Start date: June 2003
Phase: Phase 2
Study type: Interventional

The purpose of the Strongest Families (formerly Family Help Program)is to evaluate the effectiveness of the Strongest Families distance intervention compared to usual or standard care that is typically provided to children with mild to moderate Enuresis diagnoses. This is a single-centre trial based at the IWK Health Centre. The primary outcome is change in diagnosis.

NCT ID: NCT00245479 Completed - Nocturnal Enuresis Clinical Trials

A Study of Oral Desmopressin in Previously Untreated Children Aged 5 to 15 Years With Primary Nocturnal Enuresis

DRIP
Start date: April 2002
Phase: Phase 4
Study type: Interventional

To evaluate the overall response to desmopressin treatment among previously untreated enuretic children aged 5-15 years after 3 and 6 months of treatment. To investigate the influence of possible predictive factors on response after 3 and 6 months of treatment. To evaluate the proportion of patients achieving dryness. To evaluate the long-term safety profile of oral desmopressin in children with primary nocturnal enuresis.

NCT ID: NCT00240812 Completed - Enuresis Clinical Trials

A Study to Determine if Ibuprofen in Combination With Pseudoephedrine HCl is More Effective Than Each Drug Alone in the Treatment of Nighttime Bedwetting

Start date: n/a
Phase: Phase 2
Study type: Interventional

The purpose of the study is to determine if ibuprofen in combination with pseudoephedrine HCl in the treatment of nightime bedwetting in children is more effective than each drug alone and if the individual drugs are more effective than placebo.

NCT ID: NCT00239824 Completed - Clinical trials for Urinary Incontinence

Pelvic Floor Muscle Training to Treat Urinary Incontinence After Radical Prostatectomy

Start date: October 2005
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the effect of pelvic floor muscle training in the treatment of urinary incontinence after radical prostatectomy.