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N/A Completed N=57

The Effect Of Methylphenıdate Treatment On Neuroınflammatıon Levels In Chıldren Wıth Attentıon Defıcıt Hyperactıvıty Dısorder

Attention Deficit Disorder With Hyperactivity (ADHD)
Source: ClinicalTrials.gov NCT07041333 ↗
Enrolled (actual)
57
Serious AEs
0.0%
Results posted
Feb 2026
Primary outcomePrimary: Change in IL-6 Marker Level — 113.89; 103.45 ng/L — p=0.014

Summary

The aim of this study was to investigate the effect of treatment of ADHD with methylphenidate on neuroinflammation by examining the levels of Interleukin-6 (IL-6), S100B, Claudin-5 in serum samples of patients who were diagnosed with attention deficit hyperactivity disorder (ADHD) and started or planned to start methylphenidate for treatment as per routine, at month 0 before the initiation of methylphenidate treatment and at month 3 after the initiation of treatment.

Outcome Measures

OutcomeResultp-value
PRIMARY
Change in IL-6 Marker Level
113.89; 103.45 0.014 sig
PRIMARY
Change in S100B Marker Level
871.13; 758.13 0.018 sig
PRIMARY
Change in the Level of Claudin-5 Marker
206.52; 181.76 0.175

Eligibility Criteria

Inclusion Criteria

  • According to DSM-5 TR, the participant must have a diagnosis of "Attention Deficit Hyperactivity Disorder" and have started/be planning to start routine methylphenidate treatment.
  • The participant must be between 6 and 11 years of age.
  • The participant must agree to participate in the study after being informed about it.

Exclusion Criteria

  • The presence of a psychiatric disorder diagnosis other than Attention Deficit Hyperactivity Disorder
  • Having a diagnosis of Attention Deficit Hyperactivity Disorder but not planning to start methylphenidate
  • Being under 6 years of age or over 11 years of age
  • Having organic brain damage, mental retardation, autism spectrum disorder, neurological disease, or a physical illness that affects neurocognitive functions
  • History of alcohol and/or psychoactive substance use
  • Presence of ongoing active infection, allergic disease, and chronic illness
  • Previous use of psychiatric medication.
  • Presence of chronic illness
  • Regular use of medication
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT07041333). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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