Levetiracetam, Lacosamide and Ketamine as Adjunctive Treatment of Refractory Status Epilepticus

NCT ID: NCT02726867

Last Updated: 2017-08-29

Basic Information

• Recruitment Status: WITHDRAWN
• Clinical Phase: PHASE3
• Study Classification: INTERVENTIONAL
• Study Start Date: 2014-02-28
• Study Completion Date: 2016-11-30

Brief Summary

The purpose of the study is to evaluate the efficacy and safety of levetiracetam , lacosamide and ketamine treatment of refractory status epilepticus. This will be a randomized, open-label, four-arm pilot study comparing time to cessation of refractory status epilepticus, determined by continuous EEG monitoring, in patients with refractory status epilepticus. Patients with status epilepticus who have been treated with standard dose lorazepam (or midazolam) and ≥ 1000 mg phenytoin with documented levels of ≥20 mg/ml and continue to have clinical status epilepticus for ≥1-24 hours after phenytoin loading will receive intravenously (i.v.) either 4000 mg levetiracetam, 600 mg lacosamide (Group B), 2.5 mg/kg ketamine or phenobarbital 15 mg/kg phenobarbital (Group D)

Detailed Description

40 18-70 year old men and women with refractory status epilepticus, defined as status epilepticus continuing for >1 hour after completion of standard treatment with lorazepam (or midazolam) and i.v. phenytoin (or fos-phenytoin),will be enrolled. Participants will be randomized into four treatment arms, levetiracetam 4000 (Group A, n=10), lacosamide 600 mg (Group B, n=10), ketamine 2.5 mg/kg (group C,n=10),and phenobarbital 15 mg/kg (Group D, n=10) in a 1:1:1:1 ratio. Baseline evaluations will include continuous EEG, phenytoin levels prior to study intervention, CBC, CMP, serum Ca, Po4 and Mg.

Treatment will consist of levetiracetam 4000 mg i.v. over 10 minutes, lacosamide 600 mg i.v. over 10 minutes, ketamine 2.5 mg/kg over 10 minutes, or phenobarbital 15 mg/kg mg i.v. at 100 mg/minute rate.

Participants will be evaluated with ongoing physical examination and continuous EEG monitoring. Continuous EEG monitoring will be started before initiation of the study treatment, with documentation of electrographic status epilepticus. It will continue throughout the treatment period. Subjects will be observed for 1 hour clinically and with continuous EEG monitoring for cessation of SE. Participants in whom status epilepticus stops within 60 minutes of completion of study treatment will continue to receive phenytoin (150 mg i.v. q 12 hours, standard dose) and the study medication (levetiracetam 1500 mg i.v. q 12 hourly, lacosamide 300 mg q 12 hourly, ketamine 50 mg qid (vs. 40 mcg/kg/min i.v. infusion, as clinically applicable, or phenobarbital 90 mg i.v. q 12 hourly). Continuous EEG monitoring will continue for 72 hours to monitor for relapse of status epilepticus. Participants in whom status epilepticus fails to stop within 60 minutes after completion of study treatment ("non-responders") will undergo standard treatment with medically-induced coma, with intubation/ventilation and i.v. midazolam or propofol treatment at a dose to be titrated to EEG effect of "burst suppression" or suppression of all background activity. All patients, responders and non-responders alike, will continue treatment with phenytoin i.v., 150 mg q 12 hourly or, for conscious patients, 300 mg p.o. qhs for 72 hours after completion of study treatment. In patients requiring medical coma after study treatments (non-responders), medical coma will be discontinued after 48 hours. All participants will continue to be monitored with continuous EEG for 72 hours from completion of study treatment. If status epilepticus returns during this time, medical coma will be re-instituted and patients will be treated according to standard clinical care for prolonged SE

Conditions

Epilepsy; Status Epilepticus

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

levetiracetam

Patients with status epilepticus who have been treated with standard dose lorazepam (or midazolam) and ≥ 1000 mg phenytoin with documented levels of ≥20 mg/ml and continue to have clinical SE for ≥1-24 hours after phenytoin loading will receive intravenously (i.v.) 4000 mg levetiracetam.

Group Type: ACTIVE_COMPARATOR

levetiracetam

Intervention Type: DRUG

Treatment will consist of LEV 4000 mg i.v. over 10 minutes.

lacosamide

Patients with status epilepticus who have been treated with standard dose lorazepam (or midazolam) and ≥ 1000 mg phenytoin with documented levels of ≥20 mg/ml and continue to have clinical SE for ≥1-24 hours after phenytoin loading will receive intravenously (i.v.) 600 mg lacosamide.

Group Type: ACTIVE_COMPARATOR

lacosamide

Intervention Type: DRUG

Treatment will consist of LCM 600 mg i.v. over 10 minutes

ketamine

Patients with status epilepticus who have been treated with standard dose lorazepam (or midazolam) and ≥ 1000 mg phenytoin with documented levels of ≥20 mg/ml and continue to have clinical SE for ≥1-24 hours after phenytoin loading will receive intravenously (i.v.) 2.5 mg/kg ketamine.

Group Type: ACTIVE_COMPARATOR

Ketamine

Intervention Type: DRUG

Treatment will consist of KET 2.5 mg/kg over 10 minutes

phenobarbital

Patients with status epilepticus who have been treated with standard dose lorazepam (or midazolam) and ≥ 1000 mg phenytoin (PHT) with documented levels of ≥20 mg/ml and continue to have clinical SE for ≥1-24 hours after PHT loading will receive intravenously (i.v.) phenobarbital 15 mg/kg.

Group Type: ACTIVE_COMPARATOR

Phenobarbital

Intervention Type: DRUG

Treatment will consist of PHB 15 mg/kg mg i.v. at 100 mg/minute rate

Interventions

levetiracetam

Treatment will consist of LEV 4000 mg i.v. over 10 minutes.

Intervention Type: DRUG

lacosamide

Treatment will consist of LCM 600 mg i.v. over 10 minutes

Intervention Type: DRUG

Ketamine

Treatment will consist of KET 2.5 mg/kg over 10 minutes

Intervention Type: DRUG

Phenobarbital

Treatment will consist of PHB 15 mg/kg mg i.v. at 100 mg/minute rate

Intervention Type: DRUG

Other Intervention Names

Keppra; Vimpat; Ketalar; Phenobarb

Eligibility Criteria

Inclusion Criteria

1. Age 18-70

2. Ability and willingness by surrogates to signed informed consent form.

3. Clinically and electrographically documented ongoing SE lasting ≥1 hour- ≤24 hours

Exclusion Criteria

1. Creatinine > 2.5 mg/dl

2. Any systemic illness or unstable medical condition that might pose additional risk, including: cardiac, metabolic or endocrine disturbances, renal or liver disease

3. Active drug or alcohol dependence or any other factors that, in the opinion of the site investigators would interfere with adherence to study requirements

4. Pregnancy

5. Inability or unwillingness of subject or legal surrogate to give written informed consent

6. Known allergy to a study drug

7. Hypo- or hyperglycemia as cause of SE

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Mid-Atlantic Epilepsy and Sleep Center, LLC

OTHER

Sponsor Role: lead

Responsible Party

Pavel Klein

M.D.

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Pavel Klein, M.D.

Role: PRINCIPAL_INVESTIGATOR

Mid-Atlantic Epilepsy and Sleep Center

Locations

MidAtlantic Epilepsy and Sleep Center

Bethesda, Maryland, United States

Countries

United States

Other Identifiers

MAES-003

Identifier Type: -

Identifier Source: org_study_id