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Attention-Deficit Hyperactivity Disorder (ADHD) Study With Adults



Attention-Deficit Hyperactivity Disorder (ADHD) Study With Adults

For Condition: Attention Deficit Disorder
Status: Completed
Sponsor(s): Sponsor Name Pending ,
Synopsis: A placebo controlled study evaulating the efficacy and safety of medication in adults with Attention-Deficit Hyperactivity Disorder (ADHD)
Details:
Eligibility:
Study Type:
  Interventional, Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study
Minimum Age/Maximum Age: 18 Years/60 Years
Genders: Both
Protocol Entry Criteria: Inclusion Criteria: (Patients must meet the following criteria in order to be eligible for this study.) - Patient must be diagnosed with ADHD Exclusion Criteria: (Patients cannot meet the following criteria in order to be eligible for this study.) - Patient has a current or past history of seizure disorder, brain injury, anorexia nervosa or bulimia. - Patient has a current diagnosis of Major Depressive Disorder (MDD). - Patient has a current primary diagnosis of, or received treatment for, Panic Disorder, Obsessive Compulsive Disorder (OCD), Posttraumatic Stress Disorder (PTSD) or Acute Stress Disorder within the previous 12 months, - Patient has a lifetime diagnosis of bipolar disorder, schizophrenia or other psychotic disorders. - Patient has a positive urine test at screening for presence of illicit drugs or alcohol abuse during the past 12 months.
Total Enrollment: 

Location and Contact Information:

Study Site
Spring Valley,  California,  91978
United States
 

Study Site
Omaha,  Nebraska,  68105
United States
 

Study Site
Boston,  Massachusetts,  02114
United States
 

Study Site
Northridge,  California,  91324
United States
 

Study Site
Phoenix,  Arizona,  85051
United States
 

Study Site
Portland,  Oregon,  97209
United States
 

Study Site
Houston,  Texas,  77007
United States
 

Study Site
Lafayette,  California,  94549
United States
 

Study Site
Salt Lake City,  Utah,  84132
United States
 

Study Site
Burlington,  Vermont,  05405
United States
 

Study Site
Worcester,  Massachusetts,  01655
United States
 

Study Site
Rockville,  Maryland,  20852
United States
 

Study Site
Seattle,  Washington,  98104
United States
 

Study Site
Chapel Hill,  North Carolina,  27514
United States
 

Study Site
Beachwood,  Ohio,  44122
United States
 

Study Site
Woodstock,  Vermont,  05091
United States
 

Study Site
West Palm Beach,  Florida,  33407
United States
 

Study Site
Paducah,  Kentucky,  42003
United States
 

Study Site
Bellaire,  Texas,  77401
United States
 

Study Site
Cincinnati,  Ohio,  45267-0559
United States
 

Study Site
Chula Vista,  California,  91910
United States
 


Additional Information:
Study ID Numbers:
  AK130934; 
Study Start Date: 
Record last reviewed: January 2004
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00048360

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