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NMDA Receptor Antagonist

IV Ketamine for Epilepsy

Phase 2
Recruiting
Led By Madeline Fields, MD
Research Sponsored by Madeline Fields
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Established diagnosis of Drug Resistant Epilepsy (DRE) i.e. failed two or more appropriately chosen anti-seizure medications (ASMs)
Adults (18 years or older)
Must not have
Patients that are immobile i.e. wheel chair bound, bed ridden individuals
Patients <18 years of age
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 3 months post infusion
Awards & highlights
Approved for 5 Other Conditions
All Individual Drugs Already Approved
No Placebo-Only Group

Summary

This trial is testing small doses of ketamine to help people with epilepsy who don't respond to regular medications. Ketamine can help calm the brain and reduce seizures. The study will monitor patients' seizure activity and mood over time. Ketamine has been used in various settings for its ability to reduce seizures.

Who is the study for?
This trial is for adults with drug-resistant epilepsy, having more than four seizures per month. They must have a stable use of seizure devices and anti-seizure medications for specific periods before the study starts. Excluded are pregnant or breastfeeding women, those at risk of suicide or homicide, with unstable illnesses, under 18 years old, substance misuse history within two years, certain cardiovascular conditions, immobility issues or recent severe seizures.
What is being tested?
The trial tests if low doses of IV Ketamine can help control seizures in outpatients with epilepsy that doesn't respond to standard drugs. It's exploring whether this approach used in hospitals for continuous seizures can be effective when patients aren't hospitalized.
What are the potential side effects?
While not specified here, common side effects of subanesthetic ketamine may include confusion, hallucinations, changes in blood pressure and heart rate, dizziness and nausea. Long-term effects are unclear since it's usually used short-term.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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My epilepsy hasn't improved after trying two different medications.
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I am 18 years old or older.
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I experience more than 4 seizures of any type per month.
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My epilepsy device settings have been stable for at least 4 weeks.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
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I am unable to walk and use a wheelchair or stay in bed.
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I am under 18 years old.
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I have a heart condition.
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I have a history of aneurysm, aortic dissection, arteriovenous malformation, or brain bleed.
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I am taking medications for my mental health, such as amphetamines or MAO inhibitors.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~3 months post infusion
This trial's timeline: 3 weeks for screening, Varies for treatment, and 3 months post infusion for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Number of participants with seizure reduction
Seizure frequency
Secondary study objectives
General Anxiety Disorder 7-item questionnaire (GAD-7)
Neurological Disorders Depression Inventory for Epilepsy (NDDI-E) Score
Quality of Life in Epilepsy (QOLIE-10)

Side effects data

From 2020 Phase 4 trial • 75 Patients • NCT03156504
1%
Lightheadedness with low blood pressure
1%
Pump Malfunction
1%
PTSD
100%
80%
60%
40%
20%
0%
Study treatment Arm
Ketamine

Awards & Highlights

Approved for 5 Other Conditions
This treatment demonstrated efficacy for 5 other conditions.
All Individual Drugs Already Approved
Therapies where all constituent drugs have already been approved are likely to have better-understood side effect profiles.
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

1Treatment groups
Experimental Treatment
Group I: IV Ketamine HydrochlorideExperimental Treatment1 Intervention
dose 0.5mg/kg of IV Ketamine Hydrochloride over 40 min
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Ketamine
FDA approved

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for epilepsy work through various mechanisms to stabilize neuronal activity and prevent seizures. Sodium channel blockers, such as carbamazepine and phenytoin, inhibit repetitive firing of neurons by stabilizing the inactive state of sodium channels. GABA enhancers, like benzodiazepines and barbiturates, increase the inhibitory effects of GABA neurotransmission, reducing neuronal excitability. NMDA receptor antagonists, such as ketamine, inhibit excitatory neurotransmission by blocking NMDA receptors, which are involved in synaptic plasticity and excitatory signaling. Understanding these mechanisms is crucial for epilepsy patients as it helps tailor treatments to individual needs, manage side effects, and explore new therapeutic options like subanesthetic ketamine, which may offer benefits for drug-resistant epilepsy.

Find a Location

Who is running the clinical trial?

Madeline FieldsLead Sponsor
Madeline Fields, MDPrincipal InvestigatorIcahn School of Medicine
Lara Marcuse, MDPrincipal InvestigatorIcahn School of Medicine

Media Library

Ketamine Hydrochloride (NMDA Receptor Antagonist) Clinical Trial Eligibility Overview. Trial Name: NCT05019885 — Phase 2
Epilepsy Research Study Groups: IV Ketamine Hydrochloride
Epilepsy Clinical Trial 2023: Ketamine Hydrochloride Highlights & Side Effects. Trial Name: NCT05019885 — Phase 2
Ketamine Hydrochloride (NMDA Receptor Antagonist) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05019885 — Phase 2
~0 spots leftby Dec 2024