Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00141050 · ClinicalTrials.gov registry record · Phase 3

Safety and Efficacy Study of Dexmethylphenidate in Children With ADHD

A Phase 3 study, sponsored by Novartis.

Completed
Registry status
Phase 3
Development phase
90
Enrollment target

NCT00141050: Completed Phase 3 study, sponsored by Novartis.

NCT00141050 is a Phase 3 study that has completed, run by Novartis. The registered enrollment target is 90 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (88% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00141050, a Phase 3 study, has completed, sponsored by Novartis.

COMPLETED
Registry status
Phase 3
Development phase
90 participants
Enrollment target

Study Summary

The purpose of this study is to compare the safety and efficacy of two doses of dexmethylphenidate to two doses of an approved, long-acting, marketed medication for ADHD (MPH) and placebo in children ages 6-12 diagnosed with ADHD.

Interventions

  • DRUG Focalin XR

Trial Details

FieldValue
Enrollment Target 90 participants
Start Date 2005-05
Est. Completion 2005-07
Phase Phase 3
Novartis

265 total trials

What the finished NCT00141050 record still lists

NCT00141050 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 90 participants, a relatively small participant target, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (88% lower).

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

NCT00141050 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00141050 about?

NCT00141050 is a clinical study titled "Safety and Efficacy Study of Dexmethylphenidate in Children With ADHD". The purpose of this study is to compare the safety and efficacy of two doses of dexmethylphenidate to two doses of an approved, long-acting, marketed medication for ADHD (MPH) and placebo in children ages 6-12 diagnosed with ADHD.

What is the current status of trial NCT00141050?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 90 participants. The study started on 2005-05. Estimated completion is 2005-07.

What interventions are being tested in trial NCT00141050?

The interventions under investigation include: Focalin XR (DRUG).

Who is sponsoring clinical trial NCT00141050?

This trial is sponsored by Novartis, which has 265 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00141050's enrollment target sits among peer trials

90 1724th of 2000 higher than 263 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02521311 · 90 participants · Phase 2

    Assessment of Clemastine Fumarate as a Remyelinating Agent in Acute Optic Neuritis (ReCOVER)

  • NCT02939573 · 90 participants · Phase 2

    A Randomized Multicenter Study for Isolated Skin Vasculitis

  • NCT03128879 · 90 participants · Phase 2

    Venetoclax With Ibrutinib or Acalabrutinib in Pts. With High-risk CLL

  • NCT03184038 · 90 participants · NA

    Neurocognition in Patients With Multiple Brain Metastases Treated With Radiosurgery

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00141050, the US trial registry maintained by the National Library of Medicine. NCT00141050 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.