Compliance Survey of ADHD Medication for Optimal Satisfaction (COSMOS)

This study has been completed.

Sponsor:

Information provided by:

Johnson & Johnson Taiwan Ltd

ClinicalTrials.gov Identifier:

NCT00460720

First received: April 13, 2007

Last updated: April 26, 2010

Last verified: April 2010

History of Changes

No Study Results Posted on ClinicalTrials.gov for this Study

About Study Results Reporting on ClinicalTrials.gov

Study Status:	This study has been completed.
Study Completion Date:	February 2006
Estimated Primary Completion Date:	No date given

No publications provided by Johnson & Johnson Taiwan Ltd

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):

Chou WJ, Chou MC, Tzang RF, Hsu YC, Gau SS, Chen SJ, Wu YY, Huang YF, Liang HY, Cheng H. Better efficacy for the osmotic release oral system methylphenidate among poor adherents to immediate-release methylphenidate in the three ADHD subtypes. Psychiatry Clin Neurosci. 2009 Apr;63(2):167-75.

Gau SS, Chen SJ, Chou WJ, Cheng H, Tang CS, Chang HL, Tzang RF, Wu YY, Huang YF, Chou MC, Liang HY, Hsu YC, Lu HH, Huang YS. National survey of adherence, efficacy, and side effects of methylphenidate in children with attention-deficit/hyperactivity disorder in Taiwan. J Clin Psychiatry. 2008 Jan;69(1):131-40.

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