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.
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
- Conditions the study is for
- Attention Deficit/Hyperactivity Disorder, ADHD
- 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
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.
- Conditions
- Attention Deficit/Hyperactivity Disorder, ADHD
- 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.
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.
- First posted22 Sep 2005 (estimated)
- Study startSep 2003
- Primary completionSep 2006
- Study completionSep 2006
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Attention Deficit/Hyperactivity DisorderStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Cephalon
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
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
Study at a glance
From the registry record, last updated by the sponsor on 26 Jul 2012. Recruitment status is as the sponsor reported it: confirm with the study team.
- 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)
- ClinicalTrials.gov ID
- NCT00214981
- Acronym / sponsor ID
- C1538D/312/AD/US
- Conditions
- Attention Deficit/Hyperactivity Disorder, ADHD
- Keywords
- ADHD, Attention Deficit/Hyperactivity Disorder
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- Completed
- Lead sponsor
- CephalonIndustry (pharma, biotech, devices)
- Study start
- Sep 2003
- Primary completion
- Sep 2006 (actual)
- Study completion
- Sep 2006 (actual)
- First posted
- 22 Sep 2005 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Primary objective of this study is to evaluate the safety of treatment with modafinil film-coated tablet.
Study design
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Single group
- Masking
- None (open label)
Who may qualify
- Ages
- 6 to 17 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Modafinil | Drug | – |
Primary outcome
Evaluate the safety of treatment with the modafinil film coated tablet.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 26 Jul 2012.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
57 sites in 1 country: see every site and its status.
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.