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NCT07594652RecruitingPhase 4

Medication Treatment of ADHD in Pediatric Epilepsy

Use of JornayPM® to Treat ADHD in Pediatric Epilepsy

Source: ClinicalTrials.gov · Last updated 29 Jul 2026

Brief summary (registry, in English)

This is an observational study assessing the usage of stimulant medication for ADHD in the context of pediatric epilepsy.

Status (registry)
Recruiting
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
25 (estimated)
First submitted
12 May 2026
Start date
29 May 2026
Primary completion date
31 Dec 2030
Lead sponsor
Hugo W. Moser Research Institute at Kennedy Krieger, Inc.
Diseases
Epilepsy
NCT number
NCT07594652

What you commit to

  • Study type: Interventional · Phase 4
  • Planned participants: 25
  • From 29 May 2026 to the primary completion date, 31 Dec 2030
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • • Previous allergic or hypersensitivity reactions to stimulant medicines including Jornay PM®
    • Active substance abuse or dependence within 30 days of enrollment
    • Epilepsy that is unstable or with seizure frequency that exceeds four events per month, based on an average over the previous three months
    • DSM-V diagnosis of psychotic illness or imminent risk of harm to self or others.
    • Current use of stimulants to treat ADHD
    • Serious or unstable medical or neurologic conditions such as HIV, liver or kidney disease, cancer or diabetes.
    • Unstable cardiac illness such as arrythmias or cardiomyopathy.
    • Participation in a previous experimental drug study within 30 days of baseline visit.
    • Estimated IQ\<70 as indicated by clinical assessment to the degree that rating scales may be invalid
    • Insufficient capacity of caregiver or legal guardian to understand and appropriately consent for study procedures

Who the study is looking for

  • Inclusion criteria:
    • Established diagnosis of epilepsy that requires treatment with anti-seizure medication.
    • No episodes of seizure clusters or status epilepticus within 30 days prior to entry into the study.
    • Diagnosis of ADHD with functional impairment.
    • Good general health as determined by medical history and physical examination, including stable vital signs.
    • Participant or legal caregiver capable of providing informed consent and fully capable of monitoring the subject's disease process and compliance with treatment.

Age in the registry: 6 years to 17 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Kennedy Krieger Institute
Coordinator of this site? Confirm its status
BaltimoreUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.