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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00989950
Other study ID # cox002
Secondary ID shire IND#54,732
Status Completed
Phase N/A
First received September 30, 2009
Last updated July 16, 2012
Start date December 2009
Est. completion date February 2011

Study information

Verified date July 2012
Source Cox Health Systems
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

Methylphenidate may improve sleep in children with ADHD. By leaving Daytrana (methylphenidate) patch for a longer time then 9 hours, many children report short sleep latencies and better quality of sleep.


Description:

Once the optimal dose of Daytrana that controlled the ADHD symptoms is established. The patch will be removed 1, 2, and 3 hours before bed time in a random fashion, at weekly intervals, and parents will keep a sleep diary.

25 patients will be enrolled in order to obtain statistical significance.


Recruitment information / eligibility

Status Completed
Enrollment 26
Est. completion date February 2011
Est. primary completion date February 2011
Accepts healthy volunteers No
Gender Both
Age group 6 Years to 12 Years
Eligibility Inclusion Criteria:

- ADHD without significant comorbidity

Exclusion Criteria:

- Cardiac disorder

- Hypertension

- Thyroid disease

- Glaucoma

- History of sudden death, motor tics and/or Tourette's syndrome

- Hypersensitivity to methylphenidate

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Related Conditions & MeSH terms

  • Attention Deficit Disorder with Hyperactivity
  • Attention Deficit Hyperactivity Disorder
  • Hyperkinesis
  • INSOMNIA

Intervention

Drug:
Daytrana
Daytrana patch 10-30 mg administered once daily for 9hr
Daytrana
Daytrana 10-30 mg worn once daily for 10 hr wear
Daytrana
Daytrana 10-30 mg worn once daily for 11 hr
Daytrana
Daytrana 10-30 mg worn once daily for 12 hrs

Locations

Country Name City State
United States Pediatric Neurology of the Ozarks Springfield Missouri

Sponsors (1)

Lead Sponsor Collaborator
Cox Health Systems

Country where clinical trial is conducted

United States, 

References & Publications (1)

Ashkenasi A. Effect of transdermal methylphenidate wear times on sleep in children with attention deficit hyperactivity disorder. Pediatr Neurol. 2011 Dec;45(6):381-6. doi: 10.1016/j.pediatrneurol.2011.09.003. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Sleep Latency Measure by daily subject sleep diary 9 weeks No
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