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Risperidone in preschool ADHD

Risperidone in comparison with Methylphenidate in the Treatment of Preschool Children with Attention Deficit Hyperactivity Disorder

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201012205427N1
Enrollment
33
Registered
2011-03-11
Start date
2008-04-30
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. Hyperkinetic disorders

Interventions

Intervention 1: Methylphenidate(tab 10 mg) was started at a dose of 2.5 mg per day and gradually (every week) increased based on the therapeutic response and the patient’s tolerance. The optimal dose
Treatment - Drugs
Methylphenidate(tab 10 mg) was started at a dose of 2.5 mg per day and gradually (every week) increased based on the therapeutic response and the patient’s tolerance. The optimal dose of methylphenida
Risperidone was started at dose of 0.25 mg per day and increased 0.5 mg/d in the first 2 weeks (in 2 divided doses), then gradually (every two weeks) increased based on the therapeutic response and to

Sponsors

Behavioral Sciences Research Center, Shaheed Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 6 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age 3-6 years, presence of ADHD rating scale score more than 20 at the baseline Exclusion criteria: presence of any physical disease, any comorbid psychiatric disorders (for example: mood disorders, anxiety disorders, tic disorders, pervasive developmental disorders), mental retardation (IQ < 70), receiving any drug or other treatment over 2 month prior to the study

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
ADHD ratinig scale- parent. Timepoint: every 2 weeks: at the baseline, week 2, week 4, and week 6. Method of measurement: ADHD rating scale score.;Conners' Rating Scale-parent. Timepoint: every 2 weeks: at the baseline, week 2, week 4, and week 6. Method of measurement: Conners' Rating Scale score.

Secondary

MeasureTime frame
Side effects. Timepoint: every 2 weeks:every 2 weeks: week 2 (T1), week 4 (T2) and week 4 (T3). Method of measurement: intensity and frequency of side effects by using questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFariba Arabgol

Shaheed Beheshti University of Medical Sciences

farabgol@sbmu.ac.ir and faribaarab@yahoo.com+98 21 7755 1023

Outcome results

None listed

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