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Recruiting NCT06497647

NCT06497647 New Treatment for Nocturnal Enuresis in Children

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Clinical Trial Summary
NCT ID NCT06497647
Status Recruiting
Phase
Sponsor Sohag University
Condition Nocturnal Enuresis in Children
Study Type INTERVENTIONAL
Enrollment 450 participants
Start Date 2024-03-01
Primary Completion 2024-09

Eligibility & Interventions

Sex All sexes
Min Age 6 Years
Max Age 18 Years
Study Type INTERVENTIONAL
Interventions
SulbutiamineImipramine

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 450 participants in total. It began in 2024-03-01 with a primary completion date of 2024-09.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The aim of the study is to evaluate the role of sulbutiamine in treatment of monosymptomatic nocturnal enuresis in children by using it alone or as a combination therapy with tricyclic antidepressants (imipramine+sulbutiamine).

Eligibility Criteria

Inclusion Criteria: * Age : 6 - 18 years old. * All children diagnosed by Primary monosymptomatic nocturnal enuresis in this age group. Exclusion Criteria: * Secondary nocturnal enuresis (child who has been continent for at least 6 months before the onset of bedwetting ). * congenital anomalies (Posterior urethral valve , ectopic ureter , ectopia vesica ,…) * history of previous lower urinary tract surgery (Multiple hypospadias surgeries ,…, ) * neurogenic bladder (as underactive bladder ).and urge incontinence. * presence of post-void residual urine greater than 20% of functional bladder capacity. * history or evidence of disorders in other organs such as (cardiovascular system disease), liver , psychological problems , evident allergic reaction to both medication.

Contact & Investigator

Central Contact

loai mohammed abd alhamied, resident

✉ loaimohamed519@yahoo.com

📞 01093873434

Frequently Asked Questions

Who can join the NCT06497647 clinical trial?

This trial is open to participants of all sexes, aged 6 Years or older, up to 18 Years, studying Nocturnal Enuresis in Children. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06497647 currently recruiting?

Yes, NCT06497647 is actively recruiting participants. Contact the research team at loaimohamed519@yahoo.com for enrollment information.

Where is the NCT06497647 trial being conducted?

This trial is being conducted at Sohag, Egypt.

Who is sponsoring the NCT06497647 clinical trial?

NCT06497647 is sponsored by Sohag University. The trial plans to enroll 450 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology