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NCT05851391: RESTORE
buRst-supprESsion TO Stop Refractory Status Epilepticus Post-cardiac Arrest
Phase 2 trial testing Burst Suppression EEG Target Intravenous Anesthesia in Hypoxia-Ischemia, Brain in 30 participants. Currently enrolling.
30 November 2026
Quick facts
| Lead sponsor | University of California, San Francisco |
|---|---|
| Phase | Phase 2 |
| Status | Recruiting now |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 30 |
| Start date | 7 August 2023 |
| Primary completion | 30 November 2026 |
| Estimated completion | 30 April 2027 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Burst Suppression EEG Target Intravenous Anesthesia — full drug profile →
- Seizure Suppression EEG Target Intravenous Anesthesia — full drug profile →
Conditions studied
- Hypoxia-Ischemia, Brain — all drugs for Hypoxia-Ischemia, Brain →
- Heart Arrest — all drugs for Heart Arrest →
- Status Epilepticus — all drugs for Status Epilepticus →
- Refractory Status Epilepticus — all drugs for Refractory Status Epilepticus →
Sponsor
University of California, San Francisco
Who can join
18 and older, any sex, with Hypoxia-Ischemia, Brain or Heart Arrest. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
RESTORE is a randomized clinical trial investigating the safety and feasibility of using EEG treatment targets (burst suppression vs. seizure suppression) for post-cardiac arrest refractory status epilepticus treatment.
Publications & conference data
2 peer-reviewed publications reference this trial (live from Europe PMC):
-
Advances in Therapies to Treat Neonatal Hypoxic-Ischemic Encephalopathy.
Ranjan AK, Gulati A. · · 2023 · cited 41× · PMID 37892791 · DOI 10.3390/jcm12206653 -
Anesthetics in status epilepticus: does one size fits it all?-A scoping review on titration goals, timing, and patient selection.
Fisch U, De Stefano P, Baumann SM, Rüegg S, et al · · 2026 · PMID 42051778 · DOI 10.3389/fneur.2026.1805775
Verify or expand the search:
- PubMed search for NCT05851391
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT05851391 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by University of California, San Francisco
- Last refreshed: 15 May 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05851391.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing