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Dose-Finding Study to Evaluate the Efficacy and Safety of Modafinil as Treatment for Adults With ADHD
NCT00315276 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of the study is to evaluate the efficacy and safety of modafinil administered once daily for 9 weeks at doses of 255, 340, 425, and 510 mg as treatment for adults with ADHD.
Conditions Studied
Interventions
- DRUG Modafinil
Study Locations (18)
California
- Bay Area Research Institute — Lafayette
- Pharmacology Research Institute — Northridge
- Peninsula Research Associates — Rolling Hills Estates
- UCSD Medical Center — San Diego
Arkansas
- Neurology Clinical Study Centers, LLC — Little Rock
Florida
- Clinical Neuroscience Solution, Inc. — Orlando
Illinois
- University of Illinois — Chicago
Kentucky
- Michael J. Reiser, MD, LLC — Lexington
Maryland
- Adult ADD Center of Maryland — Lutherville
Massachusetts
- Massachusetts General Hospital — Cambridge
Michigan
- Rochester Center for Behavioral Medicine — Rochester
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 370 participants |
| Start Date | 2006-05 |
| Est. Completion | 2007-01 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00315276
The ClinicalTrials.gov registry entry for NCT00315276 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 370 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Cephalon, which has 17 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 2 conditions, with Attention Deficit Hyperactivity Disorder appearing as the primary indexed condition, and to 1 intervention — of which Modafinil is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT00315276 reports 18 study locations spanning 15 distinct geographic areas — top geographies include California, Arkansas, Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT00315276 about?
NCT00315276 is a clinical study titled "Dose-Finding Study to Evaluate the Efficacy and Safety of Modafinil as Treatment for Adults With ADHD". The purpose of the study is to evaluate the efficacy and safety of modafinil administered once daily for 9 weeks at doses of 255, 340, 425, and 510 mg as treatment for adults with ADHD.
What is the current status of trial NCT00315276?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 370 participants. The study started on 2006-05. Estimated completion is 2007-01.
What conditions does trial NCT00315276 study?
This clinical trial studies the following conditions: Attention Deficit Hyperactivity Disorder, ADHD. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT00315276?
The interventions under investigation include: Modafinil (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00315276?
This trial is sponsored by Cephalon, which has 17 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT00315276 being conducted?
This trial has 18 study locations across Arkansas, California, Florida, Illinois, Kentucky. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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