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Not Yet RecruitingNCT06665880

Genes, Proteins, and Metabolites in Drug-resistant Epilepsy (DRE) Patients

The Changes of Genes, Proteins, and Metabolites in Patients with Drug-resistant Epilepsy

Status
Not Yet Recruiting
Phase
Study type
Observational
Enrollment
16 (estimated)
Sponsor
Xuanwu Hospital, Beijing · Academic / Other
Sex
All
Age
14 Years – 60 Years
Healthy volunteers
Not accepted

Summary

In patients with drug-resistant epilepsy (DRE), there may be changes at the genetic, proteomic, and metabolomic levels when comparing epileptic tissues from DRE to normal tissues in traumatic brain injury (TBI). These changes could help in understanding the pathophysiological mechanisms of epilepsy and in identifying new therapeutic targets.

Detailed description

Genomical studies have identified changes in the expression of certain genes within epileptic tissues. These genes may be involved in pathways related to the balance of neuronal excitability and inhibition, synaptic transmission, and cell apoptosis. Proteomic studies will reveal changes in the abundance and modifications of proteins in epileptic tissues. These could involve proteins related to the control of neuronal excitability and synaptic transmission, such as ion channels, neurotransmitter receptors, and synaptic proteins. Metabolomic researches will reveal changes in metabolites within epileptic tissues. Epilepsy may lead to disruptions in metabolic pathways, affecting key processes such as energy metabolism, amino acid metabolism, and lipid metabolism. Sample Size: There is no minimum or maximum, but is expected to be far less than 10. In summary, patients with drug-resistant epilepsy might have changes in genes, proteomics, and metabolomics within epileptic tissues compared to normal tissue from TBI. Further research into these changes will deepen our understanding of the pathophysiology of epilepsy and guide the need for new treatment strategies.

Conditions

Interventions

TypeNameDescription
OTHERRoutine clinical treatmentRoutine clinical treatment is based on the latest international guidelines for DRE.

Timeline

Start date
2024-11-15
Primary completion
2025-12-15
Completion
2026-12-31
First posted
2024-10-30
Last updated
2024-10-30

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06665880. Inclusion in this directory is not an endorsement.