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临床试验/NCT05851391
NCT05851391招募中2 期

buRst-supprESsion TO Stop Refractory Status Epilepticus Post-cardiac Arrest (RESTORE)

University of California, San Francisco1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2023年8月7日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
招募中
入组人数
30
试验地点
1
主要终点
Post-cardiac arrest refractory status epilepticus control

研究概览

简要总结

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.

详细描述

Rationale: Seizures emerge as a complication of hypoxic-ischemic brain injury in near a third of patients successfully resuscitated from cardiac arrest. Seizures post-cardiac arrest can be refractory to treatment with anti-seizure medications and anesthetics may be used for refractory status epilepticus control. Anesthetic treatment guided by continuous EEG can target burst suppression or seizure suppression, however it is not known which strategy is superior for achieving PCARSE control.

Objective: determine the safety and feasibility of post-cardiac arrest refractory status epilepticus (PCARSE) treatment using EEG goals for intravenous anesthetic titration (burst suppression vs. seizure suppression).

Clinical Trial Phase: II

Study Design: prospective, randomized, open-label, blinded end-point, concurrently-controlled, parallel arms design clinical trial.

Study Period: two years

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Age ≥18 years old
  • •Non-traumatic, out-of-hospital cardiac arrest
  • •Comatose on admission - defined as not following commands
  • •Return of spontaneous circulation (ROSC) within less than 45 minutes
  • •Admission to the intensive care unit
  • •Diagnosis of post-cardiac arrest refractory status epilepticus confirmed with continuous
  • •EEG monitoring within 7 days from ROSC

排除标准

  • •Acute cerebral hemorrhage or infarction

研究组 & 干预措施

Burst Suppression EEG Target

Other

Anesthetic will be titrated to achieve burst suppression on continuous EEG (50-99% attenuation/suppression) for 24 hours.

干预措施: Burst Suppression EEG Target Intravenous Anesthesia (Drug)

Seizure Suppression EEG Target

Other

Anesthetic will be titrated to achieve seizure suppression on continuous EEG for 24 hours.

干预措施: Seizure Suppression EEG Target Intravenous Anesthesia (Drug)

结局指标

主要结局

Post-cardiac arrest refractory status epilepticus control

时间窗: 48 hours

Continuous EEG will be monitored to determine time to PCARSE recurrence during the anesthetic maintenance and anesthetic weaning phase (combined)

次要结局

  • Neurological Function at Discharge (CPC: Cerebral Performance Category)(30 days)
  • Seizure recurrence incidence and duration (burden)(24-48 hours)
  • PCARSE Treatment Intensity(24-48 hours)
  • Neurological Function at Discharge (mRS: modified Ranking Scale)(30 days)
  • Neurological Function 90 days (CPC: Cerebral Performance Category)(90 days)
  • Neurological Function 90 days (mRS: modified Ranking Scale)(90 days)
  • Neurological Function 180 days (mRS: modified Ranking Scale)(180 days)
  • Neurological Function180 days (mRS: modified Ranking Scale)(180 days)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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