Genetically related phenotypes of developmental epileptic encephalopathies and the mechanism of new causative genes

Status

Recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2400084478

Enrollment

Unknown

Registered

2024-05-17

Start date

2024-03-08

Completion date

Unknown

Last updated

2024-05-21

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

Conditions

epileptic encephalopathy

Interventions

Case series:NA

Eligibility

Sex/Gender

All

Age

No minimum to 14 Years

Inclusion criteria

Inclusion criteria: (i) Seizures in infancy and childhood; (ii) Seizures difficult to control by conventional antiepileptic drugs; (iii) Accompanied by backwardness, stagnation, or regression of intellectual and motor development; (iv) Abnormal EEG discharges.

Exclusion criteria

Exclusion criteria: (i) perinatal brain injury; (ii) metabolic disease; and (iii) intrauterine infection.

Design outcomes

Primary

Measure	Time frame
Whole-exome sequencing of genes;	—

Countries

China

Contacts

Public ContactHu Chunhui

Fujian Children's Hospital

huchunhui1989@126.com+86 591 8611 2178

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026