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Clinical Trials/EUCTR2006-004073-10-DE
EUCTR2006-004073-10-DE
Active, not recruiting
Not Applicable

Effect of Atomoxetine and a standardized behavior therapy on attention deficits in adult ADHD - Atomoxetine and adult ADHD

niversity of Giessen0 sitesAugust 16, 2006

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Adult Attention Deficit Hyperactivity Disorder
Sponsor
niversity of Giessen
Status
Active, not recruiting
Last Updated
14 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
August 16, 2006
End Date
TBD
Last Updated
14 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
niversity of Giessen

Eligibility Criteria

Inclusion Criteria

  • Actual diagnosis of ADHD according to DSM IV
  • Age 18 to 50
  • Both sexes
  • Declaration of informed consent for all clinical measures
  • Normal IQ (Estimated by a short IQ test during the screening)
  • Normal ECG findings
  • Sufficient knowledge of the German language to follow instructions and training procedure
  • In\- and out\-patients
  • Consent to a highly effective birth control method (failure rate less than 1%) for female patients in childbearing years
  • Are the trial subjects under 18? no

Exclusion Criteria

  • Other psychiatric disorder according to DSM IV
  • Any neurological disorder
  • Tachykardia, hyperpiesia or very low blood pressure
  • Liver malfunctions
  • Contraindication for the usage of Atomoxetine as listed in the companies safety information
  • Intake of antibiotics, azol\-antimycotics, antihistamines or antiarrhythmics
  • History of allergic reaction to Atomoxetine
  • Female patients who are pregnant or nursing
  • Other medication that affects the central nervous system
  • Paticipation in other clinical trials

Outcomes

Primary Outcomes

Not specified

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