Trials / Completed
CompletedNCT01554046
The Effect of Methylphenidate Treatment in Familial Attention Deficit/Hyperactivity Disorder (ADHD)
The Effect of Methylphenidate (Ritalin IR) Treatment in Familial Attention Deficit/Hyperactivity Disorder (ADHD)
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 40 (actual)
- Sponsor
- Sheba Medical Center · Other Government
- Sex
- All
- Age
- 6 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to investigate the familial response to Methylphenidate treatment (Ritalin IR) in two aspects: ADHD symptom's improvement and side-effects development.
Detailed description
Attention Deficit/Hyperactivity Disorder (ADHD) is very prevalent and tends to continue from childhood to adult life. It's heritability is 76%. It was found that there is a greater ADHD prevalence in first-degree families of ADHD subjects- 4-6 times more than the general population. Pharmacological treatment is the first line treatment today in ADHD, in children and adults, and Methylphenidate (specially Ritalin IR) is the first medication given for the disorder. The study includes couples of first-degree family members, both diagnosed with ADHD. Subjects will receive Ritalin IR for 4 weeks and undergo several psychiatric and cognitive questionnaires at each time of the follow-up meeting (a total of 3).
Conditions
- Attention Deficit/Hyperactivity Disorder Combined Type
- ADHD Predominantly Inattentive Type
- ADHD Predominantly Hyperactivity Type
- ADHD-not Other Specified
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Methylphenidate- Ritalin IR (Immediate Release) | Duration of treatment- 4 weeks. Dosage- up to 3 times/day. * Ages 6-12, up to 25Kg - 35mg maximum per day. * Ages 6-12, above 25Kg - 50mg maximum per day. * Ages 12-65, above 25Kg - 80mg maximum per day. |
Timeline
- Start date
- 2011-10-01
- Primary completion
- 2014-04-01
- Completion
- 2014-04-01
- First posted
- 2012-03-14
- Last updated
- 2023-12-18
Locations
1 site across 1 country: Israel
Source: ClinicalTrials.gov record NCT01554046. Inclusion in this directory is not an endorsement.