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ADHD clinical trials

View clinical trials related to ADHD.

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NCT ID: NCT00141050 Completed - ADHD Clinical Trials

Safety and Efficacy Study of Dexmethylphenidate in Children With ADHD

Start date: May 2005
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare the safety and efficacy of two doses of dexmethylphenidate to two doses of an approved, long-acting, marketed medication for ADHD (MPH) and placebo in children ages 6-12 diagnosed with ADHD.

NCT ID: NCT00061087 Completed - ADHD Clinical Trials

Treatment of Adult Attention Deficit Hyperactivity Disorder (ADHD) in Methadone Patients - 1

Start date: February 1998
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to treat Adult Attention Deficit Hyperactivity Disorder (ADHD) in methadone patients.

NCT ID: NCT00060723 Completed - ADHD Clinical Trials

Behavioral Effects of Obstructive Sleep Apnea in Children

Start date: August 1999
Phase: N/A
Study type: Observational

Sleep-disordered breathing (SDB) in children may be responsible for disruptive daytime behaviors such as inattention and hyperactivity. Many children undergo tonsillectomy for SDB and disruptive daytime behaviors. However, the link between SDB and disruptive behavior is not clearly understood. This study will evaluate the relationship between SDB and disruptive behavior.

NCT ID: NCT00046059 Completed - ADHD Clinical Trials

Genetic Analysis of Attention Deficit Hyperactivity Disorder (ADHD)

Start date: February 8, 2000
Phase:
Study type: Observational

Attention Deficit Hyperactivity Disorder (ADHD) is the most common behavioral disorder in childhood, affecting 3-5% of children between the ages of 7 and 17. Family studies suggest that there is a genetic component to ADHD. Scientists believe that it is a complex disorder in which two or more genes may be involved. Potentially eligible families will be asked to give written consent to participate and will be asked to complete questionnaires for each member in the family. In addition, an interview will be administered to the parent of minors enrolled in the study to determine their eligibility for being in the study. This screening tool is computerized and will take approximately 45 minutes to administer per child. Once screenings are completed, a blood collection kit will be sent to the family to take to their local medical care provider, have blood samples drawn and sent to NIH. There is no cost to the family to participate. We would like to enroll entire families, with both parents and all children. ...