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A Study of Dexstromethorphan Therapy for Febrile Status Epilepticus Patients against Acute Encephalopathy with Biphasic Seizures and Late Reduced Diffusion and Prevention for Residual Disability

A Study of Dexstromethorphan Therapy for Febrile Status Epilepticus Patients against Acute Encephalopathy with Biphasic Seizures and Late Reduced Diffusion and Prevention for Residual Disability - A Study of Dexstromethorphan Therapy for Febrile Status Epilepticus Patients against Acute Encephalopathy with Biphasic Seizures and Late Reduced Diffusion and Prevention for Residual Disability

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000030238
Enrollment
40
Registered
2018-02-28
Start date
2018-02-28
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

febrile status epilepticus

Interventions

Patient filling inclution criteria are started on Dextromethrophan 2mg/kg/day within 6hours after status epilepticus for 5 days.

Sponsors

Tokyo Medical and Dental University Department of Pediatrics
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The subjects are patients who meet following three inclusion criteria 1) Patients who are 6 months of age more but less than 3 years of age 2) Patients with status epilepticus(patients have convulsion more than 15 minutes) 3)Patients whose convulsion could not been stoped quickly using the first choise therapy(diazepam or midazoram) and the second choise therapy(phenytoin)(However, in regard to using continuous idazoram infusion, the case using as a second choise and failing to stop convulsion meets criteria)

Exclusion criteria

Exclusion criteria: The sujects are patients who meet following five exclusion criteria 1) Patients who are clearly suspitious of intracranial infection, cranial tumor and intracranial vascular lesion 2) patients who are clearly cranial hemorrhage for head MRI and CT in 1 or 2 days after occuring status epilepticus 3) Patients Who are acute necrotizing encephalopathy 4) Patients who already take antiepileptic drugs against epilepsy 5) Patients who already take dextromethrophan against upper respiratory infection

Design outcomes

Primary

MeasureTime frame
Primary outcome are occuring second seizures and consiousness disorder in 3-7 days after first seizure.

Secondary

MeasureTime frame
Secondary outcomes are age(between six months and one year versus between one and three years), sex, duration of seizure(less than 45 minutes versus more than 45 minutes), past history(whether patients experience feblire seizure or not), and value of AST and blood suger at admission.

Countries

Japan

Contacts

Public ContactKengo Moriyama

Tokyo Medical and Dental University Department of Pediatrics

kmoriyama.ped@tmd.ac.jp03-3813-6111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026