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Effectiveness of etentalin, Ahura hyperactive and risperidone syrups in preschool children with attention deficit hyperactivity disorder

Evaluation of the effectiveness of etentalin, Ahura hyperactive and risperidone syrups in preschool children with attention deficit hyperactivity disorder (ADHD)

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20160530028182N9
Enrollment
57
Registered
2022-12-01
Start date
2022-04-09
Completion date
Unknown
Last updated
2023-02-07

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

Conditions

Attention Deficit Hyperactive Disorder(ADHD). Attention-deficit hyperactivity disorder, predominantly hyperactive type

Interventions

Intervention 1: Intervention group: The patients included in the study during a period of 8 weeks are divided into three groups, the first group of Etentaline syrup (the first week 0.25 ml once a day,

Sponsors

Sanandaj University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 6 Years

Inclusion criteria

Inclusion criteria: The age range of these children is 3 to 6 years According to the DSM-5 diagnostic criterion, the child and adolescent psychiatrist should diagnose ADHD in children.

Exclusion criteria

Exclusion criteria: The presence of a serious physical illness, such as a seizure, based on parental history and clinical suspicion Existence of comorbid psychiatric disorder other than confrontational disobedience disorder Mental retardation based on clinical suspicion Taking medications for Attention Deficit Hyperactivity Disorder in the last month History of allergy to ethenalin and Ahura hyperactive

Design outcomes

Primary

MeasureTime frame
Parent’s ADHD Rating scale Number. Timepoint: At the beginning of the study (baseline), 2 weeks, 4 weeks and 8 weeks after the study. Method of measurement: Parent’s ADHD Rating scale.;Clinical Global Impressions Number. Timepoint: At the beginning of the study (baseline), 2 weeks, 4 weeks and 8 weeks after the study. Method of measurement: Clinical Global Impressions.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSoliman Mohammadzadeh

Sanandaj University of Medical Sciences

Dr.mohammadzadeh86@muk.ac.ir0098874957

Outcome results

None listed

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