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Evaluating effects of Cyproheptadine and Folic acid in children with ADHD receiving Ritalin

Evaluating and comparison of Cyproheptadine and Folic acid effects on appetite and hyperactivity and attention deficiency in children with ADHD receiving Ritalin

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201203167462N5
Enrollment
40
Registered
2012-04-22
Start date
2012-04-18
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 (ADHD). Disturbance of activity and attention

Interventions

Intervention 1: Intervention group1: Methyl phenidate (Ritlin: 1mg/kg) combined with Cyproheptadin (Razi: 12 mg/day- 4mg before each meal). Intervention 2: Intervention group2: Methyl phenidate (Ritli
Treatment - Drugs
Intervention group1: Methyl phenidate (Ritlin: 1mg/kg) combined with Cyproheptadin (Razi: 12 mg/day- 4mg before each meal)
Intervention group2: Methyl phenidate (Ritlin: 1mg/kg) combined with Folic acid (Alhavi: 5 mg/day)

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
7 Years to 12 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Age range of 7-12; ADHD combined form; Clinical need to treat with Methylphenidate; parental consent and child ascent Exclusion criteria: any confounding co-morbiditis; any drug supplements or narcotics consumption; Children with history of major prenatal complications such as prematurity, low birth weight (reported by parents), any past or present psychosis, comorbid tourette syndrome, celiac, phenylketonuria, autism, or other persistent developmental disorders

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Attention deficiency score and Hyperactivity score. Timepoint: 0-2-4-8 weeks. Method of measurement: ADHD rating scale for children (complited by parents).;Appetite score. Timepoint: 0-2-4-8 weeks. Method of measurement: Standard appetite questionnaire for chilldren.;Sleep disorders score. Timepoint: 0-2-4-8 weeks. Method of measurement: Sleep disorders scale for chilldren (SDSC).

Secondary

MeasureTime frame
Stimulants side effects. Timepoint: week 8. Method of measurement: Stimulants side effects questionnare.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyed Ali Mostafavi

Tehran University of Medical Sciences

mostafavi.n80@hotmail.com00

Outcome results

None listed

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