Trial Name:

Attention-Deficit/Hyperactivity Disorder (ADHD), Adults

Intro: This research study will examine how atomoxetine (Scrattera) in the treatment of ADHD in adults and how ADHD affects family functioning. Eligible participants who meet screening criteria will be closely monitored with frequent clinical visits with a physician
Condition:
Description: This research study will examine how atomoxetine (Scrattera) in the treatment of ADHD in adults and how ADHD affects family functioning. Eligible participants who meet screening criteria will be closely monitored with frequent clinical visits with a physician. Clinical care, evaluations, medications and laboratory tests done as part of the research study will be provided at no cost to the participant.
Criteria: Participants must be between 18 and-55 years of age, be in a relationship with a person of the opposite sex and have a biological child between 6-12 years old living with them.
Contact: For information or to register for screening in this trial please call HealthMatch at (216) 844-5000, or complete and submit the form below.

Participant Confidentiality:

All information regarding participation in Clinical Trials is treated with the utmost confidentiality. University Hospitals Case Medical Center and the Division of Clinical Research recognize and respect the confidentiality of this information. Access to information related to clinical trials and their participants is restricted to authorized clinical trials personnel only.

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