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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00684931
Other study ID # CHUBX 2007/21
Secondary ID
Status Terminated
Phase N/A
First received May 22, 2008
Last updated June 22, 2009
Start date February 2008
Est. completion date July 2008

Study information

Verified date June 2009
Source University Hospital, Bordeaux
Contact n/a
Is FDA regulated No
Health authority France: Direction Générale de la Santé
Study type Interventional

Clinical Trial Summary

The aim of this study is to investigate the integrity of connectivity between the neocortex and the cerebellum in the Attention Deficit Hyperactivity Disorder (ADHD). Fibers integrity will be measured using magnetic Resonance Imaging Techniques.


Description:

ADHD is a neurodevelopmental trouble characterized by attentional deficits, impulsivity and motor hyperactivity. Morphological neuroimaging studies in ADHD children have revealed cerebellar abnormalities, however data in adults regarding cerebellum alterations are scarce. In this study we will analyse the conectivity of the cerebellum of adults ADHD patients. We will use diffusion tensor imaging (DTI) technique, and morphological data will be compared with the neuropsychological status.


Recruitment information / eligibility

Status Terminated
Enrollment 19
Est. completion date July 2008
Est. primary completion date February 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 35 Years
Eligibility Inclusion Criteria:

Patient with ADHD :

- Diagnosis of ADHD

- 18 - 35 years old

Healthy volunteer :

- 18 - 35 years old

- no ADHD diagnosed

Exclusion Criteria:

- Associated neurological or psychiatric pathologies

- Pregnant woman

- MRI counter indication

Study Design

Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Basic Science


Related Conditions & MeSH terms

  • Attention Deficit Disorder With Hyperactivity
  • Hyperkinesis

Intervention

Other:
Imaging
neuropsychological evaluation and Imaging with magnetic resonance (MRI)

Locations

Country Name City State
France Charles Perrens Hospital Bordeaux
France University Hospital Bordeaux Bordeaux

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Bordeaux

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Fractional anisotropy coefficient if fronto-cerebello-frontal loops. visite 1 No
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