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Investigating the effect of Attentalin on the severity of symptoms in children with autism spectrum disorder

Investigating the effect of Attentalin on the severity of symptoms in children with autism spectrum disorder

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20241014063360N1
Enrollment
60
Registered
2024-11-01
Start date
2024-11-02
Completion date
Unknown
Last updated
2025-01-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Autism spectrum disorder. autism spectrum disorder

Interventions

Intervention 1: Intervention group: people in this group are already receiving occupational therapy and taking risperidone, and at the same time, they are prescribed atentaline drug for two months. In

Sponsors

Arak University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 7 Years

Inclusion criteria

Inclusion criteria: Age 3 to 7 years of patients with autism spectrum disorder_informed consent of the patient's parents or legal guardian to participate in the study_have a history of using risperidone for at least 1 month_ Have a history of occupational therapy for at least 6 months_Not using drugs that interfere with attentalin _no previous use of attentaline syrup_Not having gastrointestinal diseases such as peptic ulcers_No food or drug sensitivities_No skin sensitivity to light_Do not use medications that interfere with attentaline (MAOIs, midazolam, or CNS suppressants).

Exclusion criteria

Exclusion criteria: Reluctance to participate in the study, age outside this range, reluctance to take medication, use of drugs that interfere with attentaline_previous use of etentaline syrup, gastrointestinal diseases such as peptic ulcers, food or drug allergies, skin sensitivity to light, use of drugs that interfere with attentaline (MAOIs, midazolam, or CNS suppressive drugs)

Design outcomes

Primary

MeasureTime frame
GARS3 test and CBCL test and the questionnaire of drug side effects of atentalin scores will be evaluated. Timepoint: Completion of GARS 3 and CBCL questionnaire at the beginning of the study, two weeks later and two months after the start of treatment. Method of measurement: GARS3- CBCL- Attentalin side effect.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAnita alaghemand

Arak University of Medical Sciences

alaghmand@yahoo.com+98 86 3313 4501

Outcome results

None listed

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