← Back to Clinical Trials
Recruiting NCT05756621

NCT05756621 Dual Anti-glutamate Therapy in Super-refractory Status Epilepticus After Cardiac Arrest

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT05756621
Status Recruiting
Phase
Sponsor University of Milano Bicocca
Condition Status Epilepticus
Study Type OBSERVATIONAL
Enrollment 80 participants
Start Date 2022-01-15
Primary Completion 2025-09-30

Trial Parameters

Condition Status Epilepticus
Sponsor University of Milano Bicocca
Study Type OBSERVATIONAL
Phase N/A
Enrollment 80
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2022-01-15
Completion 2025-09-30
Interventions
KetamineAny anti-epileptic and anesthetic therapy, excluding Ketamine and Perampanel

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

Brief Summary

Status epilepticus (SE) is found in 20-30% of patients in coma after cardiac arrest, is often refractory to medical therapy and is considered a negative prognostic factor. Intensity and duration of treatment of refractory and super-refractory post-anoxic SE pose the ethical dilemma between futility of treatments and, conversely, their premature suspension. A recent study by the Epilepsy Center of the San Gerardo Hospital has shown that patients with super-refractory post-anoxic SE and favorable prognostic indicators can achieve a good functional outcome in more than 40% of cases, if treated with intensive and protracted therapy. However, there is profound uncertainty about the best combination of antiseizure medications and anesthetics to use in this condition. A combined anti-glutamatergic therapy with ketamine (anti-NMDA receptor) and perampanel (anti-AMPA receptor), aimed at counteracting the excitotoxicity linked to global cerebral ischemia, could be particularly effective in the treatment of super-refractory SE with post-anoxic etiology. Preliminary results in the first 26 patients treated in the Coordinating Center of the project indicate that this therapy appears safe and highly effective (80% SE resolution, 40% good neurological outcome). The aim of the SUPER-CAT study is to investigate the efficacy and safety of combined therapy with ketamine and perampanel (dual anti-glutamatergic therapy) in patients with post-anoxic super-refractory status epilepticus, compared to other therapies, using a multi-centre, retrospective, cohort study design.

Eligibility Criteria

Inclusion Criteria: * age ≥ 18 years * patients in coma after cardio-circulatory arrest (CCA) admitted to the Intensive Care Unit and treated with target temperature management (TTM) for the first 24 hours * initiation of continuous electroencephalographic (cEEG) monitoring within 24-36 hours of CCA * diagnosis of super-refractory status epilepticus, relapsed after the first cycle of anesthetics (lasting \> 24 hours) and antiepileptic therapy, defined according to the international Salzburg criteria9 * presence of pupillary reflex present bilaterally * presence of N20 cortical response present bilaterally Exclusion Criteria: * EEG with periodic pattern (generalized periodic discharges; GPDs) * status epilepticus resolved after the first cycle of anesthetics + antiepileptics * pregnant women

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology