Is a
Clinical Study attributes
NCT Number
Health Conditions in Trial
Trial Recruitment Size
180
Trial Sponsor
Trial Collaborator
Clinical Trial Start Date
2006
0Primary Completion Date
2007
0Study Completion Date
2007
0Clinical Trial Study Type
Interventional0
Interventional Trial Purpose
Treatment0
Intervention Type
Drug0
Interventional Trial Phase
Not Applicable0
Participating Facility
Official Name
Overnight Versus Progressive Conversion of Multiple Daily Dose Enteric-Coated Divalproex to Once-Daily Divalproex Extended Release: Which Strategy is Better Tolerated by Patients With Intellectual Disabilities?0
Last Updated
September 12, 2008
0Allocation Type
Randomized0
Intervention Model
Parallel Assignment0
Masking Type
None (Open Label)0
Other attributes
Intervention Treatment
Divalproex0
Study summary
The purpose of this study is to determine whether there is any difference in side effects experienced by individuals with intellectual disorders taking Depakote DR (immediate release form) when they are switched to the extended release form (ER) overnight versus when they switch more gradually over a week.
Timeline
No Timeline data yet.
Further Resources
No Further Resources data yet.
