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NCT00347152 · ClinicalTrials.gov registry record · NA
Comparison of Immediate vs Gradual Switch to Divalproex in Adults With Intellectual Disability
A NA study, sponsored by University of Kansas.
- Completed
- Registry status
- NA
- Development phase
- 18
- Enrollment target
NCT00347152: Completed NA study, sponsored by University of Kansas.
NCT00347152 is a NA study that has completed, run by University of Kansas. The registered enrollment target is 18 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00347152, a NA study, has completed, sponsored by University of Kansas.
- COMPLETED
- Registry status
- NA
- Development phase
- 18 participants
- Enrollment target
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.
Interventions
- DRUG Divalproex
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 18 participants |
| Start Date | 2006-11 |
| Est. Completion | 2007-12 |
| Phase | NA |
What the finished NCT00347152 record still lists
NCT00347152 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 18 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).
The record links to 0 conditions, and to 1 intervention - of which Divalproex is the first listed.
NCT00347152 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00347152 about?
NCT00347152 is a clinical study titled "Comparison of Immediate vs Gradual Switch to Divalproex in Adults With Intellectual Disability". 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 ...
What is the current status of trial NCT00347152?
This trial is currently completed. It is a NA study. The enrollment target is 18 participants. The study started on 2006-11. Estimated completion is 2007-12.
What interventions are being tested in trial NCT00347152?
The interventions under investigation include: Divalproex (DRUG).
Who is sponsoring clinical trial NCT00347152?
This trial is sponsored by University of Kansas, which has 66 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00347152's enrollment target sits among peer trials
18 1863rd of 2000 higher than 130 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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