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Comparison of Duloxetine and Methylphenidate in treatment of children with Attention Deficit/ Hyperactivity Disorder

Duloxetine in comparison with Methylphenidate in treatment of children with Attention Deficit/ Hyperactivity Disorder

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2012101510363N2
Enrollment
10
Registered
2012-11-08
Start date
2012-10-22
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

Attention Deficit Hyperactivity Disorder(ADHD). Attention deficit: disorder with hyperactivity hyperactivity disorder syndrome with hyperactivity

Interventions

Intervention 1: In Duloxetine group , we will prescribe this agent for 6 weeks once daily orally at night. The dose is 15 mg/d for the first week and 30 mg/d for the next 3 weeks. If needed , we will
Treatment - Drugs
In Duloxetine group , we will prescribe this agent for 6 weeks once daily orally at night. The dose is 15 mg/d for the first week and 30 mg/d for the next 3 weeks. If needed , we will increase the do
In control group, Methylphenidate ( Ritalin ) will be given 1/2 BD in first week and TDS in second week orally ( one in morning , one in afternoon and one at the evening ). Then patients will evaluate

Sponsors

University of Social Welfare and Rehabilitation Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 12 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria : ADHD diagnosis according to DSM-IV-TR that is applied by two psychiatrists; age between 6-12 years old Exclusion criteria : mental retardation; history of heart disease; drug sensitivity; comorbidity of severe mental illnesses such as bipolar disorder, major depressive disorder, conduct disorder, psychosis; history of seizure.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Severity of ADHD symtoms. Timepoint: each two weeks. Method of measurement: ADHD rating scale/ Conners rating scale-parent form.

Secondary

MeasureTime frame
Drug side effects, severity of depressive and anxiety symptoms. Timepoint: beginning and end of trial. Method of measurement: checklist of side effects- CDI-RCMAS.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNasrin Dodangi

University of Social Welfare and Rehabilitation Sciences

na.dodangi@yahoo.com nasrin.dodangi@yahoo.com+98 21 3340 1604

Outcome results

None listed

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