Clinical trials

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Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Neural Autoantibody Prevalence in New-onset Focal Seizures of Unknown Etiology

Seizure is one of the most common symptoms in autoimmune encephalitis with neuronal surface-mediated antibodies. Interestingly, some patients may exhibit new-onset seizures as the initial manifestation without fulminant sign of encephalitis, particularly in the early stage. It is essential to recognize these patients early and to perform antibody testing, as studies have reported early immunotherapy can improve their clinical outcomes. At the same time, it is important to limit the number of patients who require testing, for the sake of specificity and cost effectiveness. Thus, this prospective, multicenter study aims to identify neural antibodies in patients with focal seizures of unknown etiology, and to create a score to preselect patients requiring autoantibody testing.

Participants needed: 300
Trial details
Age: 14-100Biological sex: AllType: ObservationalSponsor: Shen Chun-HongUpdated: Aug 27, 2025Locations: 1Duration: 1 Year
Eligibility criteria

Patients have a diagnosis of new-onset focal epileptic seizure or epilepsy and p... [+4]

Patients have other etiology of seizures, such as structure, infection, genetics... [+2]

Status: Recruiting

Idiopathic Generalized Epilepsy Syndromes

The idiopathic generalized epilepsies (IGEs) have historically included the syndromes childhood absence epilepsy (CAE), juvenile absence epilepsy (JAE), juvenile myoclonic epilepsy (JME), and epilepsy with generalized tonic-clonic seizures alone (GTCA). Recognition of the IGEs is important for clinical care, as it informs diagnosis, prevents unnecessary investigation, allows optimal selection of anti-seizure medications (ASMs), and provides prognostic guidance. According to the new ILAE definition in 2022, the study aims to describe the clinical features, electroencephalographic, imaging findings and long-term prognosis.

Participants needed: 200
Trial details
Age: 4-40Biological sex: AllType: ObservationalSponsor: Shen Chun-HongUpdated: Aug 27, 2025Locations: 1
Eligibility criteria

Patients are consecutively and prospectively enrolled from epilepsy center, with... [+3]

Other epilepsy syndromes are considered during follow-up, such as genetic genera... [+1]

Status: Recruiting

A Prospective Study to Evaluate Clinical Outcomes in Anti-LGI1 Encephalitis

Anti-leucine-rich glioma-inactivated 1 (LGI1) encephalitis has been increasingly identified as the second most common type of autoimmune encephalitis after anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis. It presents with acute or subacute onset of epileptic seizures, anterograde amnesia, behavior disturbances, sleep disorders and hyponatremia. In most patients with anti-LGI1 encephalitis, immunotherapy is successful in treating the encephalitis. However, relapses, chronic epilepsy, cognitive declines and psychiatric problems have been reported in some cases. So far, prospective studies to evaluate its clinical outcomes still remain limited. In this project, the investigators will use clinical features and advanced paraclinical examinations to prospectively investigate the clinical outcomes and the associated factors in patients with anti-LGI1 encephalitis.

Participants needed: 60
Trial details
Age: 18-100Biological sex: AllType: ObservationalSponsor: Shen Chun-HongUpdated: Aug 27, 2025Locations: 1
Eligibility criteria

Meet the 2016 consensus diagnostic criteria for anti-LGI1 encephalitis. [+2]

with the diagnosis of epilepsy, stroke, cerebral trauma, and/or other nervous sy... [+2]