Nocturnal Enuresis in ChildrenPhase 3NCT07199894
Omegapres Versus Solifenacin and Mirabegron Combination Therapy in Treatment of Primary MNE
A Phase 3 study testing Mirabegron (beta3-adrenoceptor agonist), Anticholinergics and Desmopressin (DDAVP) in people with Nocturnal Enuresis in Children, run by Mansoura University at 1 site in Egypt.
Trial summary
The goal of this clinical trial is to compare combination of Solifenacin and MIrabegron in treatment of primary mono-symptomatic nocturnal enuresis in children. It will also learn about the safety of that combination. Read more about this study
- Who is it for?
- Ages 6 to 18 years
- Conditions the study is for
- Nocturnal Enuresis in Children
- What is being tested?
- Mirabegron (beta3-adrenoceptor agonist), Anticholinergics and Desmopressin (DDAVP)
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 120 participants
- Where
- 1 siteEgypt
- Study dates
- 1 Dec 2024to 1 Feb 2026
- Phase
- Phase 3
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 6 to 18 years
- All sexes
- No healthy volunteers
- Child, Adult
Who may be able to join
- Primary mono-symptomatic nocturnal enuresis -
Who cannot join
- Bowel dysfunction Psychatric illness Respiratory sleep disorders
- -
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Egypt1 site, 1 recruiting
- Recruiting
Urology and Nephrology center - Mansoura University
Al Mansurah
About this study
Official title: A Randomized Controlled Trial Comparing Mirabegron and Solifenacin Combination Therapy Versus Desmopressin Monotherapy in Treatment of Children With Primary Mono-Symptomatic Nocturnal Enuresis
The goal of this clinical trial is to compare combination of Solifenacin and MIrabegron in treatment of primary mono-symptomatic nocturnal enuresis in children. It will also learn about the safety of that combination. The main questions it aims to answer are:
Does combination of Solifenacin and MIrabegron lower the number of wet nights? What medical problems do participants have when taking combination of Solifenacin and MIrabegron? Researchers will compare the combination to omegapress to see if the combination works better to treat primary mono-symptomatic nocturnal enuresis.
Read more
Participants will:
Take the combination or Omegapress every day for 3 months Visit the clinic once monthly for checkups and tests Keep a diary of their symptoms and the number of wet nights
Read the detailed description
Nocturnal enuresis (NE) is defined as intermittent incontinence during sleep in a child aged 5 years or more in the absence of congenital anomalies of the urinary tract or congenital or acquired defects of the central nervous system. It affects 15-20% of children aged 5 years and 1-2% of adolescents with spontaneous recovery occurs at a rate of 10-15% per year. About 75% of affected children have primary nocturnal enuresis, who never attained continence for longer than 6 months during sleep. Patients with mono-symptomatic nocturnal enuresis (MNE) do not have any other symptoms of lower urinary tract dysfunction.
The standard view of NE pathogenesis as being the result of either nocturnal polyuria or nocturnal detrusal overactivity with high arousal thresholds has become well-established, but further research now complicates the picture. First, Psychological/psychiatric problems are overrepresented in enuresis and might in a minority of cases have a causal or aggravating role. Second, Nocturnal polyuria is not always linked to vasopressin deficiency. Third, nocturnal detrusal overactivity is in itself pathogenetically heterogeneous, and could be linked to constipation. Fourth, Sleep of enuretic children might be "deep," but possibly also disturbed (by obstructed airways or a distended or contracting bladder).
Standard first line treatments for MNE are alarm therapy or desmopressin. Alarm therapy conditions the child to inhibit urination during sleep or to wake to void when the bladder is full. Desmopressin decreases the amount of overnight urine produced, thereby reducing the need to wake to void. Tricyclic antidepressants are also sometimes used for treating enuresis.
Combination therapy of desmopressin plus alarm is often taken into consideration when the patients are refractory to single treatment, have behavioral problems or frequent night-time enuresis. Anticholinergic agents (AA), such as tolterodine, oxybutynin and propiverine, can prevent involuntary detrusal contractions. They can significantly decrease urge incontinence in children. Desmopressin plus AA therapy is often used in non-responders to desmopressin monotherapy or in those with a restricted bladder capacity and thickened bladder wall.
Desmopressin is more effective and has lower rate of side effects in comparison to Oxybutynin for treatment of NE. However, it has been proved that desmopressin plus AA combination (Oxybutynin or Solifenacin) therapy has higher response rates and lower relapse rates compared with desmopressin monotherapy as first-line treatment for children with primary mono-symptomatic nocturnal enuresis (PMNE) with an acceptable tolerability profile. This can be explained by bladder reservoir dysfunction during sleep which is relatively common in MNE. This phenomenon may explain treatment failure with desmopressin, despite adequate antidiuretic response. In combination therapy, desmopressin reduces urine production and the AA allows the bladder to store more urine due to increased functional bladder capacity.
Adrenoceptors have two main groups, α and β, and several subtypes. β1-, 2- and 3-adrenoceptors have been identified in human urothelium and detrusor muscle, with β3 being highly expressed in the urinary bladder. β3-adrenoceptors have been demonstrated as the predominant subtype, with 95% of all β-adrenoceptor mRNA in the human bladder relating to this subtype; this receptor is thought to be important for mediating human detrusal relaxation. This is supported by animal studies in which β3-adrenoceptor agonists have been demonstrated to cause dose-dependent detrusal relaxation during the storage phase of the micturition cycle and to inhibit neurogenic detrusal overactivity during in vitro studies. Mirabegron, a β3-adrenoceptor agonist, improves storage function and subjective symptoms without affecting voiding function in women with OAB.
To the best of our knowledge, no study used AA plus Mirabegron for treatment of PMNE In this study, we hypothesize that the combined detrusal relaxing effect of AA and β3- adrenoceptor agonist will produce better outcome regarding number of wet nights than desmopressin monotherapy in children with PMNE.
- Conditions
- Nocturnal Enuresis in Children
- Being tested
- Mirabegron (beta3-adrenoceptor agonist), Anticholinergics, Desmopressin (DDAVP)
- Keywords
- nocturnal enuresis, Desmopressin, Mirabegron, Solifenacin, B3 agonist, Anti-cholinergic, Randomised controlled trial
- Medical subject headings
- Nocturnal Enuresis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Mirabegron (beta3-adrenoceptor agonist), AnticholinergicsDrug
Anticholinergic and B3 agonist drugs used for treatment of mono-symptomatic nocturnal enuresis
Desmopressin (DDAVP)Drug
ADH analogue in treatment of mono-symptomatic nocturnal enuresis
| Study group | Role | What they receive |
|---|---|---|
| ADH analougue monotherapy | Sham comparator | Desmopressin Receives: Drug: Desmopressin (DDAVP) |
| Anticholinergic and b3 agonist combination | Experimental | Solifenacin and Mirabegron Receives: Drug: Mirabegron (beta3-adrenoceptor agonist), Anticholinergics |
What is being measured
The primary outcome is the main question the study is designed to answer.
Percentage of improvement in number of wet nights per week
Counting number of wet nights per week before and after receiving treatment and the resulting percentage will be the primary end point.
Measured: 90 days
Secondary outcomes (1)
Number of patients who experienced side effects in response to each treatment.
Each patient will be followed up monthly during the 3 months period and surveyed for side effects. The number of patients who experienced side effects will be compared between the two groups and compare the number of patients who subsequently discontinued the treatment.
Measured: 90 days
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted30 Sep 2025
- Study start1 Dec 2024
- Primary completion1 Dec 2025 (estimated)
- Study completion1 Feb 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Nocturnal Enuresis in ChildrenStudies of the same condition, open and under way.
- More trials run by Mansoura UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 3
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 120 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Mansoura University
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07199894
- Sponsor's protocol ID
- MS.24.07.2820
- Status last verified
- Sep 2025
- First submitted
- 18 Aug 2025
- Last updated
- 30 Sep 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes
Study at a glance
From the registry record, last updated by the sponsor on 30 Sep 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Randomized Controlled Trial Comparing Mirabegron and Solifenacin Combination Therapy Versus Desmopressin Monotherapy in Treatment of Children With Primary Mono-Symptomatic Nocturnal Enuresis
- ClinicalTrials.gov ID
- NCT07199894
- Acronym / sponsor ID
- MS.24.07.2820
- Conditions
- Nocturnal Enuresis in Children
- Keywords
- nocturnal enuresis, Desmopressin, Mirabegron, Solifenacin, B3 agonist, Anti-cholinergic, Randomised controlled trial
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 120 participants (estimated)
- Lead sponsor
- Mansoura UniversityUniversity, hospital or other
- Study start
- 1 Dec 2024 (actual)
- Primary completion
- 1 Dec 2025 (estimated)
- Study completion
- 1 Feb 2026 (estimated)
- First posted
- 30 Sep 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The goal of this clinical trial is to compare combination of Solifenacin and MIrabegron in treatment of primary mono-symptomatic nocturnal enuresis in children. It will also learn about the safety of that combination. The main questions it aims to answer are:
Does combination of Solifenacin and MIrabegron lower the number of wet nights? What medical problems do participants have when taking combination of Solifenacin and MIrabegron? Researchers will compare the combination to omegapress to see if the combination works better to treat primary mono-symptomatic nocturnal enuresis.
Participants will:
Take the combination or Omegapress every day for 3 months Visit the clinic once monthly for checkups and tests Keep a diary of their symptoms and the number of wet nights
Detailed description
Nocturnal enuresis (NE) is defined as intermittent incontinence during sleep in a child aged 5 years or more in the absence of congenital anomalies of the urinary tract or congenital or acquired defects of the central nervous system. It affects 15-20% of children aged 5 years and 1-2% of adolescents with spontaneous recovery occurs at a rate of 10-15% per year. About 75% of affected children have primary nocturnal enuresis, who never attained continence for longer than 6 months during sleep. Patients with mono-symptomatic nocturnal enuresis (MNE) do not have any other symptoms of lower urinary tract dysfunction.
The standard view of NE pathogenesis as being the result of either nocturnal polyuria or nocturnal detrusal overactivity with high arousal thresholds has become well-established, but further research now complicates the picture. First, Psychological/psychiatric problems are overrepresented in enuresis and might in a minority of cases have a causal or aggravating role. Second, Nocturnal polyuria is not always linked to vasopressin deficiency. Third, nocturnal detrusal overactivity is in itself pathogenetically heterogeneous, and could be linked to constipation. Fourth, Sleep of enuretic children might be "deep," but possibly also disturbed (by obstructed airways or a distended or contracting bladder).
Standard first line treatments for MNE are alarm therapy or desmopressin. Alarm therapy conditions the child to inhibit urination during sleep or to wake to void when the bladder is full. Desmopressin decreases the amount of overnight urine produced, thereby reducing the need to wake to void. Tricyclic antidepressants are also sometimes used for treating enuresis.
Combination therapy of desmopressin plus alarm is often taken into consideration when the patients are refractory to single treatment, have behavioral problems or frequent night-time enuresis. Anticholinergic agents (AA), such as tolterodine, oxybutynin and propiverine, can prevent involuntary detrusal contractions. They can significantly decrease urge incontinence in children. Desmopressin plus AA therapy is often used in non-responders to desmopressin monotherapy or in those with a restricted bladder capacity and thickened bladder wall.
Desmopressin is more effective and has lower rate of side effects in comparison to Oxybutynin for treatment of NE. However, it has been proved that desmopressin plus AA combination (Oxybutynin or Solifenacin) therapy has higher response rates and lower relapse rates compared with desmopressin monotherapy as first-line treatment for children with primary mono-symptomatic nocturnal enuresis (PMNE) with an acceptable tolerability profile. This can be explained by bladder reservoir dysfunction during sleep which is relatively common in MNE. This phenomenon may explain treatment failure with desmopressin, despite adequate antidiuretic response. In combination therapy, desmopressin reduces urine production and the AA allows the bladder to store more urine due to increased functional bladder capacity.
Adrenoceptors have two main groups, α and β, and several subtypes. β1-, 2- and 3-adrenoceptors have been identified in human urothelium and detrusor muscle, with β3 being highly expressed in the urinary bladder. β3-adrenoceptors have been demonstrated as the predominant subtype, with 95% of all β-adrenoceptor mRNA in the human bladder relating to this subtype; this receptor is thought to be important for mediating human detrusal relaxation. This is supported by animal studies in which β3-adrenoceptor agonists have been demonstrated to cause dose-dependent detrusal relaxation during the storage phase of the micturition cycle and to inhibit neurogenic detrusal overactivity during in vitro studies. Mirabegron, a β3-adrenoceptor agonist, improves storage function and subjective symptoms without affecting voiding function in women with OAB.
To the best of our knowledge, no study used AA plus Mirabegron for treatment of PMNE In this study, we hypothesize that the combined detrusal relaxing effect of AA and β3- adrenoceptor agonist will produce better outcome regarding number of wet nights than desmopressin monotherapy in children with PMNE.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| ADH analougue monotherapy | Sham comparator | Drug: Desmopressin (DDAVP)Desmopressin |
| Anticholinergic and b3 agonist combination | Experimental | Drug: Mirabegron (beta3-adrenoceptor agonist), AnticholinergicsSolifenacin and Mirabegron |
Who may qualify
- Ages
- 6 to 18 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult
Key inclusion criteria (1 listed)
- Primary mono-symptomatic nocturnal enuresis -
Key exclusion criteria (2 listed)
- Bowel dysfunction Psychatric illness Respiratory sleep disorders
- -
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Mirabegron (beta3-adrenoceptor agonist), AnticholinergicsAnticholinergic and B3 agonist drugs used for treatment of mono-symptomatic nocturnal enuresis | Drug | Anticholinergic and b3 agonist combination |
| Desmopressin (DDAVP)ADH analogue in treatment of mono-symptomatic nocturnal enuresis | Drug | ADH analougue monotherapy |
Primary outcome
Percentage of improvement in number of wet nights per week
Time frame: 90 days
Counting number of wet nights per week before and after receiving treatment and the resulting percentage will be the primary end point.
1 secondary outcome
Number of patients who experienced side effects in response to each treatment.
Time frame: 90 days
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 30 Sep 2025.
- Individual participant dataSharing planned: Yes
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Potential Adjuvant Therapies for Children With Primary Nocturnal Enuresis
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing Mirabegron (beta3-adrenoceptor agonist), Anticholinergics and Desmopressin (DDAVP) in people with Nocturnal Enuresis in Children, run by Mansoura University at 1 site in Egypt.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 30 Sep 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Abdelhamid El Sayed Shahin, MBBCH (+201005876463, hameedshahin95@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Percentage of improvement in number of wet nights per week (time frame: 90 days). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 Sep 2025.