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Comparison of two regimens in the treatment of nocturnal enuresis

Comparison of treatment of monosymptomatic nocturnal enuresis with combination of Desmopressin and Tolterodin versus Desmopressin alone

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2012090610758N1
Enrollment
100
Registered
2012-09-24
Start date
2012-04-04
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Primary nocturnal enuresis. Nonorganic enuresis

Interventions

Intervention 1: In two-drug regimen group: Tolterodin 2 mg/day orally plus nasal Desmopressin 1 puff/night for 4 weeks. Intervention 2: In one-drug regimen group: nasal Desmopressin 1 puff/night and
Treatment - Drugs
In two-drug regimen group: Tolterodin 2 mg/day orally plus nasal Desmopressin 1 puff/night for 4 weeks
In one-drug regimen group: nasal Desmopressin 1 puff/night and placebo with the same shape, size and color of the Tolterodin once per night orally for 4 weeks

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
5 Years to 16 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: (having primary nocturnal enuresis; not having secondary nocturnal risk factors such as urinary tract infection, constipation, Diabetes Mellitus, Diabetes Insipidus, obstruction of the urinary tract, neurogenic bladder and positive history of seizure; to be between 5 to 16 years old) Exclusion criteria: (having abnormal sonographic or urine analysis results; occurrence of side effects or missing the intake of more than two doses of the prescribed drugs)

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Frequency of nocturnal urination in a week. Timepoint: weekly for four weeks. Method of measurement: Using a questionnaire.

Secondary

MeasureTime frame
Occurrence of side effects. Timepoint: Weekly for four weeks. Method of measurement: Physical examination by a specialist.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAdorreza Otofat

Tabriz University of Medical Sciences

dr.otofat@yahoo.com+98 41 1658 4305

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026