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Comparing efficacy and side effects of Memantine and Risperidone in treating autistic patients

Comparing efficacy and side effects of Memantine and Risperidone in treating autistic patients

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201204037202N5
Enrollment
30
Registered
2012-06-20
Start date
2012-06-21
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

Autism. Pervasive developmental disorders

Interventions

Intervention 1: Risperidone with gradual increasing in dose will be prescribed as bellow: 0.02mg/kg/day at begining, 0.04 mg/kg/day at second week and ultimately will be increased to 0.06 mg/kg/day at
Treatment - Drugs
Risperidone with gradual increasing in dose will be prescribed as bellow: 0.02mg/kg/day at begining, 0.04 mg/kg/day at second week and ultimately will be increased to 0.06 mg/kg/day at third week. Cal
Memantine with gradual increasing in dose will be prescribed as bellow: 0.2mg/kg/day at begining, 0.3mg/kg/day at second week and ultimately will be rised to 0.4mg/kg/day at third week. Calculated dos

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
4 Years to 17 Years

Inclusion criteria

Inclusion criteria: inclusion criteria: age of 4-17 year old; autistic patients not received any drug for treatment in past or not responded adequately to previous drugs; seizure attacks in epileptic patients should be controlled and any change in dose and kind of antiepileptic drugs should not be made from one month before entrance to the study. exclusion criteria: any neurologic disease except for seizure; substance abuse; pregnancy; any history of neuroleptic malignant syndrom and history of allergic reactions to mementine or risperidone; history of cardiovascular diseases, malignant hematologic diseases, acute kidney or liver failure.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Autism symptoms. Timepoint: before intervention, four and eight weeks after intervention. Method of measurement: Aberrant Behavioral Check list and Childhood Autism Rating Scale scales.

Secondary

MeasureTime frame
Side effects including any side effect that related to the drug. Timepoint: two, four and eight weeks after intervention. Method of measurement: side effects checklist.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNaemeh Nikvarz

Tehran University of Medical Sciences

nnikvarz@yahoo.com+98 21 6695 4709

Outcome results

None listed

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