buRst-supprESsion TO Stop Refractory Status Epilepticus Post-cardiac Arrest
Launched by UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · May 1, 2023
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
The RESTORE trial is a research study looking at new ways to help patients who have seizures after a cardiac arrest, known as refractory status epilepticus. The trial is exploring two different treatment approaches: one that aims to reduce the activity in the brain called "burst suppression" and another that focuses on stopping seizures. This study is important because it could lead to better care for patients who are in a coma after cardiac arrest and are not responding to standard treatments.
To participate in this trial, patients must be at least 18 years old and have experienced a cardiac arrest outside of the hospital. They should be in a coma when they arrive at the hospital and have had their heart restarted within 45 minutes. Participants will receive close monitoring in the intensive care unit, and their brain activity will be continuously checked to confirm the diagnosis of refractory status epilepticus. It's important to note that patients with certain conditions, such as bleeding in the brain or those who are pregnant, cannot join the study. If you or a loved one qualifies, this trial could offer access to innovative treatments that may improve recovery outcomes.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Age ≥18 years old
- • 2. Non-traumatic, out-of-hospital cardiac arrest
- • 3. Comatose on admission - defined as not following commands
- • 4. Return of spontaneous circulation (ROSC) within less than 45 minutes
- • 5. Admission to the intensive care unit
- • 6. Diagnosis of post-cardiac arrest refractory status epilepticus confirmed with continuous
- • EEG monitoring within 7 days from ROSC
- Exclusion Criteria:
- • 1. Acute cerebral hemorrhage or infarction
- • 2. Pregnancy
- • 3. Prisoners
About University Of California, San Francisco
The University of California, San Francisco (UCSF) is a leading academic institution renowned for its commitment to advancing healthcare through innovative research and clinical trials. With a focus on translating scientific discoveries into effective therapies, UCSF collaborates with a diverse array of stakeholders, including healthcare professionals, industry partners, and patient communities. The university's research programs emphasize interdisciplinary approaches and leverage cutting-edge technology to address complex medical challenges. As a sponsor of clinical trials, UCSF is dedicated to maintaining the highest standards of ethical conduct and scientific rigor, ensuring the safety and well-being of participants while contributing to the broader medical knowledge base.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
San Francisco, California, United States
Patients applied
Trial Officials
Edilberto Amorim, MD
Principal Investigator
Assistant Professor of Neurology
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported