NCT06966830

Brief Summary

Status epilepticus (SE) is an acute and critical form of neurological and systemic diseases involving multiple clinical disciplines, with an annual incidence of (20-73) per 100,000 people and a clinical case fatality rate of 20%. Although there are many causes of SE, the primary goal of treatment is to terminate the seizures quickly, and timely and standardized treatment can reduce mortality and improve prognosis. The prognosis is closely related to the duration of the episode, and the longer the episode, the worse the prognosis. If seizures of convulsive status epilepticus persist for more than 10 minutes and are not provided with optimal therapeutic intervention, serious adverse outcomes and even death are likely to occur. How to effectively terminate status epilepticus and actively find effective, reliable and safe treatment options is a key research problem at present. Due to critical illness, limited treatment options, and poor prognosis, new treatments are urgently needed to terminate persistent epileptic activity. Lacosamide (LCM) is a third-generation new antiepileptic drug, which was approved in 2008 for the additive treatment of patients aged 16 years and older with focal seizures, with or without generalized seizures. In 2017, it was extended to patients over 4 years of age. Lacosamide is an anticonvulsant drug with a new dual mechanism of action: first, lacosamide antagonizes the glycine site of N-methyl-D-aspartate (NMDA) receptor; Second, lacosamide selectively acts on the slow inactivation of sodium channels and prolongs the inactivation time of sodium channels, which can more effectively reduce sodium influx and reduce the excitability of neurons, so as to achieve the purpose of treating epilepsy. Lacosamide exhibits linear pharmacokinetics, high oral bioavailability, protein binding of \< 15%, rapid and almost complete absorption in a single oral dose, and maximum plasma concentrations within 1 to 4 hours. A number of randomized controlled clinical studies and real-world studies abroad have shown that lacosamide can significantly improve the effective rate and seizure-free rate of epilepsy control, and it is well tolerated and has fewer adverse reactions. The 2022 Chinese Expert Consensus on the Diagnosis and Treatment of Post-stroke Epilepsy recommended lacosamide injection as a first-line drug for non-convulsive status epilepticus after stroke, and the Chinese Expert Consensus on the Diagnosis and Treatment of Status Epilepticus in Children (2022) recommended that lacosamide be considered as an additive treatment for refractory convulsive status epilepticus in children \> 60 minutes . There is a lack of clinical research data on the efficacy and safety of intravenous bolus lacosamide for status epilepticus, including convulsive status epilepticus and non-convulsive epilepticus.

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
18mo left

Started Jun 2025

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress38%
Jun 2025Oct 2027

First Submitted

Initial submission to the registry

May 4, 2025

Completed
9 days until next milestone

First Posted

Study publicly available on registry

May 13, 2025

Completed
24 days until next milestone

Study Start

First participant enrolled

June 6, 2025

Completed
1.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 30, 2027

Expected
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

October 30, 2027

Last Updated

May 30, 2025

Status Verified

May 1, 2025

Enrollment Period

1.9 years

First QC Date

May 4, 2025

Last Update Submit

May 26, 2025

Conditions

Keywords

LacosamideIntravenous InjectionEmergency TerminationEfficacy

Outcome Measures

Primary Outcomes (1)

  • Seizure reduction rate

    1. 1-hour status epilepticus termination rate after treatment; 2. seizure-free rate 24 hours after treatment; 3. 3 day seizure-free rate after treatment.

    From enrollment to the end of treatment at 1 week

Study Arms (1)

Patients with status epilepticus meets the 2015 diagnostic criteria of the ILAE

Patients with status epilepticus meets the 2015 diagnostic criteria of the International League Against Epilepsy, which is a state in which seizures are persistent and likely to cause long-term impairment, and manifests as: 1. Tonic-clonic seizures or convulsive seizures, lasting \> 5min; 2. Between 2 or more seizures, consciousness is not restored; 3. Focal seizures with impaired consciousness, lasting \>10min; 4. absence seizures, lasting \> 15min;

Drug: Lacosamide (LCM)

Interventions

Intravenous lacosamide is given for the treatment of seizure termination in patients with status epilepticus

Patients with status epilepticus meets the 2015 diagnostic criteria of the ILAE

Eligibility Criteria

Age4 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64)
Sampling MethodNon-Probability Sample
Study Population

Patients with status epilepticus who are admitted to our hospital and other 4 collaboration hospitals

You may qualify if:

  • Age 4-60 years old, gender is not limited;
  • Status epilepticus meets the 2015 diagnostic criteria of the International League Against Epilepsy, i.e., a state of persistent seizures that may cause long-term impairment and manifests itself as:
  • (1) Tonic-clonic seizures or convulsive seizures, lasting \> 5min; (2) Between 2 or more seizures, consciousness is not restored; (3) Focal seizures with impaired consciousness, lasting \>10min; (4) absence seizures, lasting \>15min; 3. Informed consent of the patient and signed a written consent form.

You may not qualify if:

  • Unstable vital signs;
  • Electrocardiogram showing atrial flutter, atrial fibrillation, second-degree, third-degree atrioventricular block;
  • History of allergy to the drugs used this time;
  • Participants have a known history of past or present illness of non-epileptic seizures, and current seizures cannot be judged as status epilepticus based on symptomatology and/or electroencephalogram;
  • Other patients who are considered by the investigator to be unsuitable to participate in the study;
  • Incomplete clinical data or follow-up information

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

The Second Affiliated Hospital of Guangzhou Medical Universty

Guangzhou, GuanDong, 510260, China

Location

Related Publications (8)

  • Hsiao MR, Tsai TC, Hsia SH, Chan OW, Lee EP, Lin JJ, Lin KL. Intravenous lacosamide for acute repetitive seizures and convulsive status epilepticus in critically ill children. Epilepsia Open. 2024 Dec;9(6):2241-2250. doi: 10.1002/epi4.13047. Epub 2024 Sep 10.

    PMID: 39254674BACKGROUND
  • Strzelczyk A, Zollner JP, Willems LM, Jost J, Paule E, Schubert-Bast S, Rosenow F, Bauer S. Lacosamide in status epilepticus: Systematic review of current evidence. Epilepsia. 2017 Jun;58(6):933-950. doi: 10.1111/epi.13716. Epub 2017 Mar 11.

    PMID: 28295226BACKGROUND
  • Rogawski MA, Tofighy A, White HS, Matagne A, Wolff C. Current understanding of the mechanism of action of the antiepileptic drug lacosamide. Epilepsy Res. 2015 Feb;110:189-205. doi: 10.1016/j.eplepsyres.2014.11.021. Epub 2014 Dec 3.

    PMID: 25616473BACKGROUND
  • Doty P, Rudd GD, Stoehr T, Thomas D. Lacosamide. Neurotherapeutics. 2007 Jan;4(1):145-8. doi: 10.1016/j.nurt.2006.10.002.

    PMID: 17199030BACKGROUND
  • Gainza-Lein M, Sanchez Fernandez I, Jackson M, Abend NS, Arya R, Brenton JN, Carpenter JL, Chapman KE, Gaillard WD, Glauser TA, Goldstein JL, Goodkin HP, Kapur K, Mikati MA, Peariso K, Tasker RC, Tchapyjnikov D, Topjian AA, Wainwright MS, Wilfong A, Williams K, Loddenkemper T; Pediatric Status Epilepticus Research Group. Association of Time to Treatment With Short-term Outcomes for Pediatric Patients With Refractory Convulsive Status Epilepticus. JAMA Neurol. 2018 Apr 1;75(4):410-418. doi: 10.1001/jamaneurol.2017.4382.

    PMID: 29356811BACKGROUND
  • Coppler PJ, Elmer J. Status Epilepticus: A Neurologic Emergency. Crit Care Clin. 2023 Jan;39(1):87-102. doi: 10.1016/j.ccc.2022.07.006. Epub 2022 Oct 7.

    PMID: 36333039BACKGROUND
  • Chin RF, Neville BG, Peckham C, Bedford H, Wade A, Scott RC; NLSTEPSS Collaborative Group. Incidence, cause, and short-term outcome of convulsive status epilepticus in childhood: prospective population-based study. Lancet. 2006 Jul 15;368(9531):222-9. doi: 10.1016/S0140-6736(06)69043-0.

    PMID: 16844492BACKGROUND
  • Rossetti AO, Alvarez V. Update on the management of status epilepticus. Curr Opin Neurol. 2021 Apr 1;34(2):172-181. doi: 10.1097/WCO.0000000000000899.

    PMID: 33664203BACKGROUND

MeSH Terms

Conditions

EpilepsyStatus Epilepticus

Interventions

Lacosamide

Condition Hierarchy (Ancestors)

Brain DiseasesCentral Nervous System DiseasesNervous System DiseasesSeizuresNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

AcetamidesAmidesOrganic ChemicalsAcetatesAcids, AcyclicCarboxylic Acids

Study Officials

  • Na He, Ph.D

    Second Affiliated Hospital of Guangzhou Medical University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

May 4, 2025

First Posted

May 13, 2025

Study Start

June 6, 2025

Primary Completion (Estimated)

April 30, 2027

Study Completion (Estimated)

October 30, 2027

Last Updated

May 30, 2025

Record last verified: 2025-05

Data Sharing

IPD Sharing
Will share

the efficacy of intravenous lacosamide in the treatment of seizure termination and electroencephalogram improvement in patients with status epilepticus

Locations