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Methylphenidate and atomoxetine in attention deficit hyperactivity disorder

Comparison of the effectiveness of methylphenidate and atomoxetine in the treatment of attention deficit hyperactivity disorder in adult patients

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20110802007202N15
Enrollment
36
Registered
2018-11-08
Start date
2018-08-01
Completion date
Unknown
Last updated
2019-01-14

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

Conditions

Attention deficit hyperactivity disorder in adults. Attention-deficit hyperactivity disorder, unspecified type

Interventions

Intervention 1: Intervention group 1: Pharmacotherapy with methylphenidate 10 milligram immediate release tablets ( Ritalin) manufactured by Novartis pharmaceutical industry in Switzerland. The medici

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
19 Years to 50 Years

Inclusion criteria

Inclusion criteria: Attention Deficit Hyperactivity Disorder Age between 19-50 years Signing consent form

Exclusion criteria

Exclusion criteria: Patients with a history of any systemic disorder such as cardiovascular diseases Patients with a history of bipolar disorder, major depressive disorder, psychosis, substance abuse, pervasive developmental disorder and intellectual disability Using psychotropic drugs within one month prior to the initiation of the study

Design outcomes

Primary

MeasureTime frame
Score of inattentive and hyperactive symptoms in Conners Adult ADHD Rating Scale - self report questionnaire. Timepoint: Before intervention and 2, 4, 6 and 8 weeks after the intervention. Method of measurement: Self report Conners Adult ADHD Rating Scale questionnaire.

Secondary

MeasureTime frame
The score of Hamilton Depression questionnaire. Timepoint: Before intervention and 8 weeks after the intervention. Method of measurement: Hamilton depression questionnaire.;The score of Hamilton Anxiety questionnaire. Timepoint: Before intervention and 8 weeks after the intervention. Method of measurement: Hamilton Anxiety questionnaire.;The score of general assessment of functioning scale. Timepoint: Before intervention and 8 weeks after the intervention. Method of measurement: General assessment of functioning scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactParya Tajmehrabi Namini

Tehran University of Medical Sciences

paryataj@yahoo.com+98 21 6693 3989

Outcome results

None listed

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