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Attention Deficit/Hyperactivity DisorderPhase 3NCT00214981

Evaluate the Safety and Efficacy of Modafinil in Children and Adolescents With ADHD

A Phase 3 study testing Modafinil in people with Attention Deficit/Hyperactivity Disorder and ADHD, run by Cephalon at 57 sites in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Primary objective of this study is to evaluate the safety of treatment with modafinil film-coated tablet. Read more about this study

Who is it for?
Ages 6 to 17 years
What is being tested?
Modafinil
How many people
Not given
Where
57 sitesUnited States
Study dates
Sep 2003to Sep 2006
Phase
Phase 3
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 6 to 17 years
  • All sexes
  • No healthy volunteers
  • Child

Inclusion Criteria: Patients are included in the study if they participated in a previous qualifying study with modafinil and, in the opinion of the investigator, will continue to benefit from treatment with modafinil. In addition, the following criteria must be met:

  • a boy or girl 6 to 17 years of age, inclusive, and English-speaking
  • weight and height between the 5th and 95th percentile on the National Center for Health Statistics (NCHS) growth chart for age, height, and weight
  • if more than 6 months since last dose of study drug, meets the full DSM-IV crieria for ADHD (combined typd, predominantly inattentive type, or predominantly hyperactive - impulsive type) at screening, as manifested by a psychiatric/clinical evaluation and confirmed by a structured diagnostic interview, namely, the Diagnostic Interview Schedule for Children, Fourth Edition (DISC-IV).
  • are in good health (except for a diagnosis of ADHD) as determined by medical and psychiatric history, physical examination, ECG, serum chemistry, hematology, urinalysis
  • girls of child bearing potential (Tanner scale >3) OR all girls 8 years of age and older have a negative urine pregnancy test at screening, must be using a medically acceptable method of birth control, and must agree to continue use of this method for the duration of the study (and for 30 days after participation in the study). (NOTE: For conducting pregnancy tests, the investigator has the option of determining the sexual maturity all girls 8 years of age and older.) Acceptable methods of birth control include: barrier method with spermicide; steroidal contraceptive (eg, oral, transdermal, implanted, and injected) in conjunction with a barrier method; intrauterine device (IUD); or abstinence
  • have a parent or legal guardian who is willing to participate in the study.

Exclusion Criteria: Patients are excluded from participating in this study if 1 or more of the following criteria are met:

  • a history or current diagnosis of pervasive developmental disorder, schizophrenia, or other psychotic disorders, or a clinical assessment of current suicide risk
  • any current psychiatric comorbidity, including but not limited to depression or other mood disorder, anxiety disorder, or pervasive mental disorder, that requires pharmacotherapy
  • a clinically significant drug sensitivity to stimulants such as amphetamine, dextroamphetamine, methylphenidate, pemoline
  • failure to respond to 2 or more adequate courses (dose or duration) of ADHD therapy
  • use of any other prescription medications for ADHD (e.g., amphetamine, dextroamphetamine, methylphenidate, pemoline, atomoxetine) after the screening visit
  • use of any MAO inhibitors or SSRIs within 2 weeks of the baseline visit
  • hypertension, defined as follows (SBP = systolic blood pressure and DBP = diastolic blood pressure):
  • ages 6-9 years SBP > 122mmHg or DBP>78mmHg
  • ages 10-12 years SBP > 126mmHg or DBP>82mmHg
  • ages 13-17 years SBP > 136mmHg or DBP>86mmHg
  • hypotension, defined as sitting systolic blood pressure (taken after resting for 5 minutes) of less than 50mmHg for children under 12 years of age or less than 80mmHg for children 12 and older
  • a sitting pulse outside the range of 60 through 115 bpm after resting for 5 minutes

Trial locations and contacts

57 sites in 1 country.

57 sites in 1 country

United States57 sites
  • Child Neurology Assoc.

    Atlanta, Georgia, 30342

  • Kentucky Pediatric/Adult Resea

    Bardstown, Kentucky, 40004

  • NeuroScience, Inc.

    Bethesda, Maryland, 20814

  • University of Alabama Birmingh

    Birmingham, Alabama, 35025

  • Foothills Psychiatry

    Boise, Idaho, 83702

  • Massachusetts General Hospital

    Boston, Massachusetts, 02114

  • Alpine Clinical Research

    Boulder, Colorado, 80304

  • University of Buffalo

    Buffalo, New York, 14214

  • Otter Creek Clinical Studies

    Burlington, Vermont, 05401

  • North Carolina Neuropsychiatry

    Chapel Hill, North Carolina, 27514

  • North Carolina Neuropsychiatry

    Charlotte, North Carolina, 28209

  • Psychiatric Professional Servi

    Cincinnati, Ohio, 45267-0559

  • CNS Research Institute

    Clementon, New Jersey, 08021

  • Dallas Pediatric Neurology

    Dallas, Texas, 75230

  • Midwest Neurology, Inc.

    Danville, Indiana, 46122

  • Mountainview Center for Resear

    Decatur, Georgia, 30033

  • OCCI Eugene

    Eugene, Oregon, 97401

  • River Valley Neurology

    Fort Smith, Arkansas, 72901

  • Sarkis Clinical Trials

    Gainesville, Florida, 32607

  • Amedica Research Inst.

    Hialeah, Florida, 33013

  • UCI Child Development Center

    Irvine, California, 92612

  • James A. Knutson, MD

    Kirkland, Washington, 98033

  • Clinical Research Center of NV

    Las Vegas, Nevada, 89014

  • Radiant Research Las Vegas

    Las Vegas, Nevada, 89146-5611

  • Michael J. Rieser, MD

    Lexington, Kentucky, 40509

  • Clinical Study Centers, LLC

    Little Rock, Arkansas, 72205

  • Children's Developmental Cente

    Maitland, Florida, 32751

  • Marshfield Clinical Research

    Marshfield, Wisconsin, 54449

  • Clinical Neuroscience Solution

    Memphis, Tennessee, 38119

  • Pivotal Research Center

    Mesa, Arizona, 85210

  • Miami Research Associates

    Miami, Florida, 33173

  • Vanderbilt University Medical

    Nashville, Tennessee, 37232

  • Dolby Providers, Inc.

    New Orleans, Louisiana, 70128

  • New York Psychiatric Inst

    New York, New York, 10032

  • Cientifica at Prarie View

    Newton, Kansas, 67114

  • Monarch Research Associates

    Norfolk, Virginia, 23510

  • Consultants in Neurology, Ltd.

    Northbrook, Illinois, 60062

  • Pahl Pharmaceutical Research

    Oklahoma City, Oklahoma, 73118

  • University of Nebraska

    Omaha, Nebraska, 68198-7630

  • Vince and Associates Clinical

    Overland Park, Kansas, 66211

  • Pedia Research, LLC

    Owensboro, Kentucky, 42301

  • Four Rivers Clinical Research

    Paducah, Kentucky, 42003

  • CNS Research Institute PC

    Philadelphia, Pennsylvania, 19149

  • Primary Physicians Research

    Pittsburgh, Pennsylvania, 15241

  • Summit Research Network Inc.

    Portland, Oregon, 97210

  • Rhode Island Hospital

    Providence, Rhode Island, 02903

  • University of Rochester

    Rochester, New York, 14642

  • OCCI, Inc.

    Salem, Oregon, 97309

  • Radiant Research Salt Lake

    Salt Lake City, Utah, 84107

  • UT Health Science Center

    San Antonio, Texas, 78229-3900

  • BMR HealthQuest

    San Diego, California, 92123

  • University of CA San Francisco

    San Francisco, California, 94143

  • Pacific Institute of Mental He

    Seattle, Washington, 98133-9009

  • Encompass Clinical Research

    Spring Valley, California, 91978

  • Children's Specialized Hospita

    Toms River, New Jersey, 08755

  • Clinical Neurophysiology Svcs

    Troy, Michigan, 48085

  • Clinical Neuroscience Solution

    West Palm Beach, Florida, 33407

Other trials in United States

About this study

Official title: A 1-Year, Open-Label, Flexible-Dosage Study to Evaluate the Safety and Continued Efficacy of Modafinil (Film-coated Tablet Formulation) in Children and Adolescents With Attention-Deficit/Hyperactivity Disorder (Followed by an Open-Ended Extension Period)

Primary objective of this study is to evaluate the safety of treatment with modafinil film-coated tablet.

Being tested
Modafinil
Keywords
ADHD, Attention Deficit/Hyperactivity Disorder
Medical subject headings
Attention Deficit Disorder with Hyperactivity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • ModafinilDrug

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Evaluate the safety of treatment with the modafinil film coated tablet.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Sep 2005 (estimated)
  2. Study startSep 2003
  3. Primary completionSep 2006
  4. Study completionSep 2006

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 3
Primary purpose
Treatment
Allocation
Non-randomised
Intervention model
Single group
Masking
None (open label)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00214981
Sponsor's protocol ID
C1538D/312/AD/US
Status last verified
Jul 2012
First submitted
14 Sep 2005
Last updated
26 Jul 2012
Results posted
No

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing Modafinil in people with Attention Deficit/Hyperactivity Disorder and ADHD, run by Cephalon at 57 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 26 Jul 2012. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 57 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Evaluate the safety of treatment with the modafinil film coated tablet.. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Jul 2012.

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