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Comparison of the Effectiveness of Hydrochlorothiazide with Nasal Spray of Desmopressin in Treatment of Nocturia in Children Referring to Pediatric Nephrology Clinic in hamadan in first 6 month of 2019

Phase 3
Recruiting
Conditions
Enuresis.
Nonorganic enuresis
Registration Number
IRCT20181212041936N1
Lead Sponsor
Hamedan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
208
Inclusion Criteria

All girls aged more than 5 years old and all boys over 6 years of age with diagnosis of primary monosymptomatic nocturnal enuresis referred to the nephrology clinic of children

Exclusion Criteria

Anatomical disorders lead to urinary incontinence such as neurogenic bladder, posterior ureteral valve and anatomical disorders of the ureter
Metabolic disorders leading to polyuria such as diabetes mellitus and diabetes insipid
secondary nocturnal enuresis
polysymptomatic nocturnal enuresis
Parental dissatisfaction
adverse effects of drugs

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Resolved of Enuresis. Timepoint: Patients are followed up for a period of 6 months, and the outcome of the disease is the drying up of the child during sleep during medication three months and within three months after it, after discontinuation of drugs, in addition to monthly monitoring during the monthly visits to the families It will be explained if the child reports wetting the next day and if the child remains dry. Meanwhile, after the discontinuation of the medications within the next three months, follow-up and drying or returning of the enuresis will be considered. Method of measurement: Completion of follow-up questionnaires.
Secondary Outcome Measures
NameTimeMethod
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