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NF1-Attention: Study of Children With Neurofibromatosis Type 1 Treated by Methylphenidate
This study is currently recruiting participants.
Verified by Hospices Civils de Lyon, October 2007
First Received: September 9, 2005   Last Updated: October 3, 2007   History of Changes
Sponsor: Hospices Civils de Lyon
Information provided by: Hospices Civils de Lyon
ClinicalTrials.gov Identifier: NCT00169611
  Purpose

Neurofibromatosis type 1 (NF1) is an autosomal dominant disorder with an estimated prevalence of 1/2190 to 1/6711. Attention deficit hyperactivity disorder (ADHD) has been reported to be common in NF1. We, the researchers at Hospices Civils de Lyon, designed a randomized, double blind, placebo controlled, crossover trial with a total follow-up duration of 9 weeks to evaluate the effect of methylphenidate (MPH) on the improvement on the simplified parents Conners' Rating Scale. In a parallel exploratory study we will compare the nature of attention deficit disorders in NF1 children to 30 ADHD NF1-free controls. Children aged 7 to 12 years are eligible when their intelligence quotient (IQ) is between 80 and 120. Fifty subjects (25 for each period) were required for testing the primary study hypothesis.


Condition Intervention Phase
Neurofibromatosis Type 1
Drug: methylphenidate
Phase IV

Study Type: Interventional
Study Design: Randomized, Double-Blind, Placebo Control, Crossover Assignment
Official Title: Comportemental and Neuropsychologic Study of Children With Neurofibromatosis Type 1 Treated by Methylphenidate. A Double-Blind Randomised Study Methylphenidate Versus Placebo

Resource links provided by NLM:


Further study details as provided by Hospices Civils de Lyon:

Primary Outcome Measures:
  • Effect of methylphenidate compared to placebo on ADHD. Time of measurements are realised on day 0, day 28, day 63 + 2 days.

Secondary Outcome Measures:
  • To evaluate the efficacy of methylphenidate compared to placebo on specific neuropsychologic, depression and anxiety scales
  • To compare the nature of attention deficit disorders in NF1 children with those with primary ADHD, depression, and anxiety using the State Trait Anxiety Inventory for Children (STAI-C) and the Children's Depression Inventory (CDI).
  • Time of measurements are realised on day 0, day 28, day 63 + 2 days.

Estimated Enrollment: 80
Study Start Date: January 2004
  Eligibility

Ages Eligible for Study:   7 Years to 12 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Age 7-12 years
  • IQ between 80-120.
  • Gender: male or female
  • Children with neurofibromatosis type 1 (according to the National Institutes of Health [NIH] 1988).
  • Patients with school difficulties pointed out by parents or teachers
  • Patients with attention difficulties as defined by anamnesis

Exclusion Criteria:

  • IQ > 120 or IQ < 80
  • Child depression
  • Unwillingness to participate
  • Patients with cerebral complication of neurofibromatosis type 1 (chiasma glioma, moya-moya) as detected by cerebral magnetic resonance imaging (MRI).
  • Participation in another study
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00169611

Contacts
Contact: Laurence LION-FRANCOIS, MD 33 4 72 38 55 54 laurence.francois@chu-lyon.fr

Locations
France
Laurence LION-FRANCOIS Recruiting
Lyon, France, 69005
Contact: Laurence LION-FRANCOIS, MD     33 4 72 38 55 54     laurence.francois@chu-lyon.fr    
Sponsors and Collaborators
Hospices Civils de Lyon
Investigators
Principal Investigator: Laurence LION-FRANCOIS, MD Hospices Civils de Lyon
  More Information

Additional Information:
No publications provided

Study ID Numbers: 2003.310
Study First Received: September 9, 2005
Last Updated: October 3, 2007
ClinicalTrials.gov Identifier: NCT00169611     History of Changes
Health Authority: France: Afssaps - French Health Products Safety Agency

Keywords provided by Hospices Civils de Lyon:
Neurofibromatosis type 1
Attention deficit with hyperactivity disorder school difficulties
methylphenidate

Additional relevant MeSH terms:
Dopamine Uptake Inhibitors
Neurotransmitter Agents
Neurotransmitter Uptake Inhibitors
Molecular Mechanisms of Pharmacological Action
Neoplasms, Nerve Tissue
Physiological Effects of Drugs
Methylphenidate
Neurodegenerative Diseases
Neurofibromatosis 1
Heredodegenerative Disorders, Nervous System
Neurofibroma
Neuromuscular Diseases
Therapeutic Uses
Neurocutaneous Syndromes
Neoplasms by Histologic Type
Nervous System Diseases
Central Nervous System Stimulants
Pharmacologic Actions
Neoplasms
Neoplastic Syndromes, Hereditary
Genetic Diseases, Inborn
Peripheral Nervous System Diseases
Neurofibromatoses
Dopamine Agents
Central Nervous System Agents
Nerve Sheath Neoplasms

ClinicalTrials.gov processed this record on February 08, 2010