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Interferential currents and desmopressin in primary nocturnal enuresis of 5-15 years old children: A Randomized clinical trial.

Interferential currents and desmopressin in primary nocturnal enuresis of 5-15 years old children: A Randomized clinical trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT138801161323N3
Enrollment
75
Registered
2009-11-21
Start date
2007-04-21
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 enuresis. Nonorganic enuresis

Interventions

Intervention 1: Nasal spray of Vasopressin, 10-20 microgram every night for three to four months and gradual tapering within 6 months. Intervention 2: 5 weeks treatment by IFC, three sessions per week
Treatment - Drugs
Treatment - Other
Nasal spray of Vasopressin, 10-20 microgram every night for three to four months and gradual tapering within 6 months
5 weeks treatment by IFC, three sessions per week for 20 minutes

Sponsors

Research management affairs, Yasuj University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
5 Years to 15 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Age 5-15 years, presence of primary nocturnal enuresis that at least had history of two times nocturnal bed wetting per week Exclusion criteria: Any history of urinary tract infections, diurnal enuresis, organic disease and abnormality of urinary systems, resistance to other treatments modalities

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Complete improvment of enuresis. Timepoint: first month every two week then monthy for 6 months. Method of measurement: observation by parents.;Partial improvment of enuresis. Timepoint: First month every two weeks and then monthly for 6 months. Method of measurement: At least 50% decrease in bed wetting observed by parents.

Secondary

MeasureTime frame
Recurrence of enuresis. Timepoint: one month after discontiuation of intervention. Method of measurement: observation by parents.;Adverse effects. Timepoint: First month every two weeks and then monthly for six months. Method of measurement: Report by patients or parents or observer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSadrollah Mehrabi

Yasuj University of Medical Sciences, Yasuj, Iran

mehrabi390@yahoo.com and dr mehrabiyums.ac.ir+98 74 1333 7228

Outcome results

None listed

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