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comparison of Memantine and Methylphenidate in the treatment of children with ADHD

comparison of memantine and ritalin in the treatment of children with ADHD

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201205157462N7
Enrollment
40
Registered
2012-06-01
Start date
2012-05-21
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

attention deficiency hyperactivity disorder. Disturbance of activity and attention

Interventions

Intervention 1: One group of patients are randomly assigned to the intervention group are treated with Memantine 10 mg. Therapeutic dosage of Memantine 10 mg is prescribed a tablet daily for the firs
in the second week, two tablets are daily prescribed (one in the morning at 8 o'clock, one at 14 o'clock)
if the weight is above 30 pounds, 3 tablets will be daily prescribed in the second week (one and a half tablet each morning at 8 o'clock, one and a half tablet at 14 o'clock).
Treatment - Drugs
One group of patients are randomly assigned to the intervention group are treated with Memantine 10 mg. Therapeutic dosage of Memantine 10 mg is prescribed a tablet daily for the first week (half tab
if the weight is above 30 pounds, 3 tablets will be daily prescribed in the second week (one and a half tablet each morning at 8 o'clock, one and a half tablet at 14 o'clock)

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 11 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: receiving DSM-IV-TR diagnostic criteria for ADHD; the age range of 6 to 11 years old; not using any psychiatric drugs at least 2 weeks before the research. Exclusion criteria: having mental retardation; having any psychiatric disorders except ODD; allergic history to Memantine; having serious disorder like heart disease; uncontrolled Seizure disorder; individuals with Systolic blood pressure above 125 mmHg or resting pulse under 60 or having above 115 beats per minute.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
The ADHD symptoms. Timepoint: Baseline, third and sixth weeks after intervention. Method of measurement: ADHD Rating Scale, Clinical Global Impressions Severity.

Secondary

MeasureTime frame
Side effects. Timepoint: Baseline, third and sixth weeks after intervention. Method of measurement: Side effects quesionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSoleiman Mohammadzadeh, MD

Tehran University of Medical Sciences, Psychiatry research center

dr.mohammadzadeh86@gmail.com+98 21 5541 3540

Outcome results

None listed

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