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UnknownNCT05229627

Multimodal Magnetic Resonance Imaging Study on the Neural Mechanisms of Remission in Children With ADHD

Multimodal Magnetic Resonance Imaging Study on the Neural Mechanisms of Remission in Children With ADHD Treated With Methylphenidate or Atomoxetine

Status
Unknown
Phase
Study type
Observational
Enrollment
250 (estimated)
Sponsor
Peking University Sixth Hospital · Academic / Other
Sex
All
Age
6 Years – 16 Years
Healthy volunteers
Accepted

Summary

Attention-deficit/hyperactivity disorder(ADHD) is highly prevalent among children and adolescents and often associated with poor long-term outcomes in adulthood. it is thus a serious public health problem. Methylphenidate(MPH) and Atomoxetine(ATX) are most frequently used for treating ADHD in many countries but the individual treatment response varies. Some patients present good response to either MPH or ATX with minimal or no symptoms left and optimal functioning(remission) after treatment, while others are poor responders to one of the two or even both. The underlying mechanism for the heterogenous responsiveness remains unknown. Thus we proposed to use multimodule magnetic resonance imaging(MRI) technology to explore the neural mechanisms of remission in children with ADHD treated with MPH or ATX.

Detailed description

the main aim of the current study is to explore the mechanism of remission in children with ADHD treated by MPH or ATX. Baseline information including demographic information, clinical features including ADHD symptoms, cognitive assessments such as executive function, MRI scans including resting state functional MRI, structural MRI, and DTI would be acquired in each participant. after 8-12 weeks of treating with MPH or ATX, patients would be classified into subgroups of remitted and unremitted groups. all baseline tests would be acquired again at the end of the study. comparisons would be done to explore the remission mechanism induced by MPH or ATX

Conditions

Interventions

TypeNameDescription
DRUGMPHthe drug would be prescribed to patients without any contraindication
DRUGATXthe drug would be prescribed to patients without any contraindication

Timeline

Start date
2016-01-01
Primary completion
2022-12-31
Completion
2023-12-31
First posted
2022-02-08
Last updated
2022-02-08

Source: ClinicalTrials.gov record NCT05229627. Inclusion in this directory is not an endorsement.