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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00372359
Other study ID # BAR1400CTIL
Secondary ID
Status Recruiting
Phase N/A
First received September 3, 2006
Last updated September 19, 2012
Start date August 2006
Est. completion date December 2012

Study information

Verified date September 2012
Source Barzilai Medical Center
Contact Shraga Aviner, MD, PhD
Phone 972 3 674 5165
Email aviners@barzi.health.govb.il
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Observational

Clinical Trial Summary

The purpose of this study is to find out whether prolonged treatment with methylphenidate has any adverse effect on cardiac functions and measurements.


Description:

Attention deficit hyperactivity disorder (ADHD) is the most common neurobehavioral condition of childhood, with symptoms consisting of inattentiveness, impulsivity and hyperactivity. The diagnosis relies on subjective criteria since there is no objective test for ADHD. Stimulants are the recommended treatment, during the last 2 decades both the rate of its use has increased, and the age for starting treatment has decreased. Adverse side effects have been few, none of which were serious.

Recently, regulators of the Food and Drug Administration (FDA) have been told on forty deaths among patients who took stimulants through 2003. Accordingly, a subcommittee of the FDA recommended that prescription drugs to treat ADHD should be accompanied by strong 'black-box' warnings that they may increase the risk of heart problems in some patients.

To date, there does not appear to have been any study that has evaluated cardiac functions in these patients. In this study we will evaluate the possible long term effect of methylphenidate on cardiac functions, as to provide more knowledgeable basis for decisions on the treatment of ADHD patients with methylphenidate.

Children age 8-18 years who were treated on methylphenidate for more then five years will be allocated in outpatient clinics. Complete EKG and echocardiographic examinations will be performed and cardiac functions, left ventricular mass and left ventricular muscle width will be compared to the normal range of values. The results will give us, for the first time, a basis to support or reject the causative relationship between these drugs and severe cardiac problems.


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date December 2012
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 8 Years to 18 Years
Eligibility Inclusion Criteria:

Children with ADHD aged 8-18 years who are taking methylphenydate (Ritalin©, Ritalin SR©, Ritalin LA©) for more than 5 years.

Exclusion Criteria:

Children with any known heart disease or anomaly. Children whose ADHD is part of a syndrome or are mentally retarded. Children that are on any other chronic medications.

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms

  • Attention Deficit Disorder
  • Attention Deficit Disorder With Hyperactivity
  • Attention Deficit Disorders With Hyperactivity
  • Attention Deficit Hyperactivity Disorder
  • Attention Deficit Hyperactivity Disorders
  • Disease
  • Hyperkinesis

Locations

Country Name City State
Israel Pediatric Day Care Center, The Barzilai Medical Center Ashkelon

Sponsors (1)

Lead Sponsor Collaborator
Ornit Cohen

Country where clinical trial is conducted

Israel, 

References & Publications (4)

Cohen AL, Jhung MA, Budnitz DS. Stimulant medications and attention deficit-hyperactivity disorder. N Engl J Med. 2006 May 25;354(21):2294-5. — View Citation

Debate over warnings for ADHD stimulants. Child Health Alert. 2006 Apr;24:1. — View Citation

Nissen SE. ADHD drugs and cardiovascular risk. N Engl J Med. 2006 Apr 6;354(14):1445-8. Epub 2006 Mar 20. — View Citation

Wooltorton E. Medications for attention deficit hyperactivity disorder: cardiovascular concerns. CMAJ. 2006 Jul 4;175(1):29. Epub 2006 Jun 13. — View Citation

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