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Effect of Vitamin D and Omega 3 in treatment of children with enuresis

Effect of Vitamin D, Omega 3 and their combination in treatment of 7-15 years old children with enuresis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015062222868N1
Enrollment
180
Registered
2015-09-09
Start date
2015-06-27
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

nocturnal enuresis. Nonorganic enuresis

Interventions

Intervention 1: intervention group1: vitamin D3 supplement 1000 IU,1 tablet per day during 2 months and omega3 placebo capsule,1 capsule per day for 2 months. Intervention 2: Intervention group 3: vi
Treatment - Drugs
intervention group1: vitamin D3 supplement 1000 IU,1 tablet per day during 2 months and omega3 placebo capsule,1 capsule per day for 2 months
Intervention group 3: vitamin D3 supplement 1000 IU,1 tablet per day during 2 months and omega3 supplement 1000 mg , 1 capsule per day for 2 months
control group: placebo tablets of vitamin D3 ,1 tablet per day for 2 months and placebo capsule of omega 3 , 1 capsule per day for 2 months
Intervention group 2: omega3 supplement 1000 mg , 1 capsule per day for 2 months and vitamin d3 placebo tablet 1 tablet per day for 2 month

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
7 Years to 15 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age between 7-15; the tendency of parents to participate in the project and signing the consent form; the diagnosis of enuresis in child exclusion criteria: high serum calcium; high ratio of urine calcium to creatinin ; diabetics;

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Nocturnal enuresis. Timepoint: every week during 2 months intervention. Method of measurement: Questionnaire.

Secondary

MeasureTime frame
Serum 1,25 (OH)2 vitaminD level. Timepoint: before study and at the end of study. Method of measurement: blood test.;Urine prostaglandin E2 level. Timepoint: before and after intervention. Method of measurement: urine test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactElham Rahmani

School Of Nutrition and Food Science

stud2300111111@sums.ac.ir+98 71 3725 1001

Outcome results

None listed

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