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Nocturnal Enuresis clinical trials

View clinical trials related to Nocturnal Enuresis.

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NCT ID: NCT01582542 Active, not recruiting - Nocturnal Enuresis Clinical Trials

Desmopressin for Improving Nocturnal Enuresis in Patients After Radical Cystectomy With Bladder Reconstruction

Start date: April 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to prospectively assess whether Desmopressin, given for a period of month to patients after radical cystectomy with orthotopic bladder reconstruction, improves and lowers the rate of nocturnal enuresis.

NCT ID: NCT01575678 Recruiting - Nocturnal Enuresis Clinical Trials

The Effect of Melatonin on Nocturnal Enuresis

Start date: January 2012
Phase: Phase 2
Study type: Interventional

Aim: To investigate the effect of melatonin in bedwetting.

NCT ID: NCT01368913 Completed - Nocturnal Enuresis Clinical Trials

MINRIN® Orally Disintegrating Tablet (Fast Dissolving Desmopressin) and Tablets in Treatment of Primary Nocturnal Enuresis

MELT
Start date: June 2011
Phase: N/A
Study type: Observational

Desmopressin in treatment of nocturnal enuresis (bedwetting).

NCT ID: NCT01078753 Completed - Nocturnal Enuresis Clinical Trials

Study With Two Different Doses of Desmopressin Orally Lyophilisate Tablet With Nocturnal Enuresis

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

This is multi-center, randomized, placebo-controlled, parallel-group, double-blind, dose-escalating clinical trial designed to assess the efficacy and safety of desmopressin orally lyophilisate for the treatment of nocturnal enuresis "with decreased nighttime urinary osmolality."

NCT ID: NCT01036841 Completed - Enuresis Clinical Trials

Influence of Food-intake on Desmopressin Oral Tablets and MELT-formulation

TM
Start date: December 2009
Phase: Phase 4
Study type: Interventional

Alarm-treatment as well as Desmopressin, a synthetic analogue of human vasopressin, are considered the only evidence-based medicine (EBM) IA treatments in monosymptomatic nocturnal enuresis (MNE). Desmopressin exists in three different formulations for ambulant use: nasal spray, tablet and lyophilisate (MELT) each with differences in bioavailability (spray 2%, tablet 0.2%, MELT 0.5%). There 's insufficient evidence to confirm the actually used bioequivalent doses ( 10µg spray = 120µg MELT= 0.2mg tablet). Although so frequently used, very few pharmacokinetic and -dynamic data on desmopressin are available for children. Due to prolonged half life, associated with waterintoxication,the nasal spray has a black box warning from the FDA and is no longer recommended . For some authors oral formulations appear to be a safer alternative. However, based on clinical experience of less response rate with oral formulations, lower biodisponibility is suspected. Adult research confirms low bioavailability of tablets but also show major influences by food-intake and changes in gastro-intestinal motility. To achieve maximum efficacy, recommendations are to take desmopressin tablet 1 hour before bedtime and 2 hours after meal: this is unrealistic in schoolaged children since there never is 3 hours between evening meal and bedtime. In 2005 a dose response study demonstrated superior pharmaco-kinetic and dynamic properties for desmopressin Lyophilisate MELT formula. Since these results implicate superior action of MELT, often a change to MELT is recommended if there is a suboptimal response with tablet: sublingual absorption would eliminate the influence of food-intake. However, for this statement there's no evidence, since these tests were all conducted in children in fasting condition. Only one clinical study demonstrates bioequivalence for MELT and tablet. Hypothesis is that desmopressin MELT formulation has a better bioavailability when administered together with meal due to its sublingual absorption.

NCT ID: NCT00404638 Not yet recruiting - Clinical trials for Monosymptomatic Enuresis Nocturna

Treatment of Enuresis Nocturna by Circular Muscle Exercise (Paula Method)

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

Several treatment modalities for children suffering from monosymptomathic nocturnal enuresis are available including drugs, alarms, acupuncture, pelvic floor training and biofeedback. The aim of this study is to to test if Paula Method (circular muscle exercise) can be an another treatment modality.

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: NCT00230594 Completed - Clinical trials for Primary Nocturnal Enuresis

Desmopressin Response in the Young

DRY
Start date: July 2004
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether desmopressin administered as a melt tablet is effective in reducing the number of wet nights in children and adolescents who suffer from bedwetting.