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NCT00195741 · ClinicalTrials.gov registry record · Phase 3

The Safety and Efficacy of Divalproex Sodium Extended-Release Tablets in Migraine Prophylaxis: A Study in Adolescents

A Phase 3 study of Migraine, sponsored by Abbott.

Completed
Registry status
Phase 3
Development phase
300
Enrollment target
1
Study location

NCT00195741: Completed Phase 3 study of Migraine, sponsored by Abbott.

NCT00195741 is a Phase 3 study of Migraine that has completed, run by Abbott. The registered enrollment target is 300 participants, below the 355-participant average among 102 other Migraine trials with a reported enrollment target (15% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00195741, a Phase 3 study of Migraine, has completed, sponsored by Abbott.

COMPLETED
Registry status
Phase 3
Development phase
300 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to determine whether Depakote ER is safe and effective in the reduction of occurrence of migraine headaches in adolescents.

Conditions Studied

Interventions

  • DRUG divalproex sodium

Study Locations (1)

Illinois

  • Global Medical Information - Abbott - North Chicago

Trial Details

FieldValue
Enrollment Target 300 participants
Start Date 2003-05
Phase Phase 3
Abbott

181 total trials

What the finished NCT00195741 record still lists

NCT00195741 is an interventional study that assigns participants to a tested intervention. The registered 300 participants enrollment target is mid-sized for trials with a published cap, below the 355-participant average among 102 other Migraine trials with a reported enrollment target (15% lower).

The record links to 1 condition, with Migraine appearing as the primary indexed condition, and to 1 intervention - of which divalproex sodium is the first listed.

NCT00195741 reports a single indexed study location in Illinois.

Frequently Asked Questions

What is clinical trial NCT00195741 about?

NCT00195741 is a clinical study titled "The Safety and Efficacy of Divalproex Sodium Extended-Release Tablets in Migraine Prophylaxis: A Study in Adolescents". The purpose of this study is to determine whether Depakote ER is safe and effective in the reduction of occurrence of migraine headaches in adolescents.

What is the current status of trial NCT00195741?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 300 participants. The study started on 2003-05.

What conditions does trial NCT00195741 study?

This clinical trial studies the following conditions: Migraine.

What interventions are being tested in trial NCT00195741?

The interventions under investigation include: divalproex sodium (DRUG).

Who is sponsoring clinical trial NCT00195741?

This trial is sponsored by Abbott, which has 181 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00195741 being conducted?

This trial has 1 study location across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Migraine

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT00195741's enrollment target sits among peer trials

300 32nd of 102 higher than 71 of 102 other Migraine trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Migraine 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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Source: ClinicalTrials.gov NCT00195741, the US trial registry maintained by the National Library of Medicine. NCT00195741 (mid enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.