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Clinical Trials/CTRI/2011/08/001981
CTRI/2011/08/001981
Completed
Phase 4

To compare the efficacy and tolerability of methylphenidate and atomoxetine in children with attention deficit hyperactivity disorder.

Department of Psychiatry0 sites69 target enrollmentTBD

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Not specified
Sponsor
Department of Psychiatry
Enrollment
69
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
May 31, 2012
Last Updated
4 years ago
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • Patients from 6 to 15 years of age with the diagnosis of Attention Deficit Hyperactivity Disorder according to Diagnostic and Statistical Manual of Mental Disorders\-IV\-Text Revision.
  • Patients with moderate to severe illness as assessed by Clinical Global Impressions Severity Scale.
  • Patients whose parents are willing to provide informed consent for participating in the study.

Exclusion Criteria

  • Patients with history of non\-response or adverse drug reactions to methylphenidate or atomoxetine in the past.
  • Patients who have taken any medication for ADHD in past one month.
  • Patients with history of heart disease, seizures, bipolar affective disorder, psychotic illness, pervasive developmental disorder, substance abuse, anxiety, mental retardation or tic disorder.

Outcomes

Primary Outcomes

Not specified

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