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NCT00434213 · ClinicalTrials.gov registry record · Phase 4

Characterization of Dermal Reactions in Pediatric Patients With ADHD Using DAYTRANA

A Phase 4 study, sponsored by Noven Therapeutics.

Completed
Registry status
Phase 4
Development phase
309
Enrollment target

NCT00434213: Completed Phase 4 study, sponsored by Noven Therapeutics.

NCT00434213 is a Phase 4 study that has completed, run by Noven Therapeutics. The registered enrollment target is 309 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (40% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00434213, a Phase 4 study, has completed, sponsored by Noven Therapeutics.

COMPLETED
Registry status
Phase 4
Development phase
309 participants
Enrollment target

Study Summary

This is a study designed to characterize the dermal response of DAYTRANA. Subjects will visit the study site over a period of approximately 14 weeks.

Primary Outcome

Dermal reactions were graded on a scale ranging from 0 (no irritation) to 7 (strong reaction) for observed findings of erythema, edema, papules, and vesicles.

Interventions

  • DRUG Daytrana

Trial Details

FieldValue
Enrollment Target 309 participants
Start Date 2007-01
Est. Completion 2008-07
Phase Phase 4
Noven Therapeutics

10 total trials

What the finished NCT00434213 record still lists

NCT00434213 is an interventional study that assigns participants to a tested intervention. The registered 309 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (40% lower).

The record links to 0 conditions, and to 1 intervention - of which Daytrana is the first listed.

NCT00434213 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00434213 about?

NCT00434213 is a clinical study titled "Characterization of Dermal Reactions in Pediatric Patients With ADHD Using DAYTRANA". This is a study designed to characterize the dermal response of DAYTRANA. Subjects will visit the study site over a period of approximately 14 weeks.

What is the current status of trial NCT00434213?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 309 participants. The study started on 2007-01. Estimated completion is 2008-07.

What interventions are being tested in trial NCT00434213?

The interventions under investigation include: Daytrana (DRUG).

Who is sponsoring clinical trial NCT00434213?

This trial is sponsored by Noven Therapeutics, which has 10 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00434213's enrollment target sits among peer trials

309 263rd of 2000 higher than 1,738 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 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 NCT00434213, the US trial registry maintained by the National Library of Medicine. NCT00434213 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.