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临床试验/NCT07835802
NCT07835802尚未招募1 期

Optimization of Neurological and Functional Recovery Following Cardiac Arrest

National Taiwan University Hospital1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2026年9月17日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
尚未招募
入组人数
100
试验地点
1
主要终点
clinical & electrical seizure occurrence

研究概览

简要总结

Sudden cardiac arrest (SCA) remains one of the major challenges in clinical care.

Although improvements in resuscitation quality have increased the likelihood of return of spontaneous circulation (ROSC), most patients still fail to survive to hospital discharge, and neurological injury is the leading determinant of poor outcome. Hypoxic-ischemic encephalopathy caused by global cerebral hypoxia during cardiac arrest is a key contributor to long-term disability, and even survivors often experience substantial functional impairment, placing a significant burden on families and society. Targeted temperature management (TTM) has long been regarded as a cornerstone neuroprotective strategy; however, TTM and TTM2 trials reported no significant neurological difference between lower and higher temperature targets. However, these studies predominantly enrolled patients with relatively mild illness severity, and multiple real-world observational cohorts suggest that, among more severely ill resuscitated patients, lower target temperatures may still confer benefit. Consequently, the optimal temperature strategy in higher-risk subgroups remains uncertain. Seizures are another common manifestation of brain injury after cardiac arrest, occurring in approximately 20-30% of resuscitated patients and contributing to secondary neurological damage. Earlier trials evaluating prophylactic anti-seizure medication (ASM) (thiopental or diazepam/magnesium) did not demonstrate neurological benefit; however, these studies primarily focused on neuroprotection rather than seizure prevention, leaving a substantial evidence gap. Patients with moderate to severe disease severity-those at the highest risk of both cerebral injury and seizure occurrence-have never been specifically studied to determine whether personalized temperature selection or early short-term prophylactic ASM (e.g., valproic acid or levetiracetam) may provide clinical benefit. Accordingly, identifying the most appropriate temperature target for higher-risk patients and determining whether short-term prophylactic antiepileptic therapy can reduce seizure-related injury represent important unresolved questions in post-resuscitation care. The aim of this study is to conduct a prospective, multicenter, randomized clinical trial to evaluate whether, among comatose patients with moderate to severe risk after ROSC, specific TTM temperature strategies combined with early short-term prophylactic ASM can reduce postresuscitation seizure incidence and improve neurological outcomes. By addressing a population underrepresented in prior clinical trials-those at highest risk and most likely to benefit-this study aims to generate clinically meaningful evidence to guide temperature selection and prophylactic ASM after cardiac arrest. Evaluating these interventions in combination may provide a more comprehensive understanding of whether they reduce seizure burden, mitigate brain injury, and improve functional recovery.

研究设计

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

入排标准

年龄范围
18 Years 至 99 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Non-traumatic sudden cardiac arrest in adults
  • •Sustained return of spontaneous circulation (ROSC) for at least 5 minutes
  • •Admitted to the intensive care unit (ICU), remaining comatose and unable to follow commands
  • •TIMECARD score indicating moderate-to-severe illness severity
  • •Randomization and initiation of the intervention can be completed within 12 hours after ROSC

排除标准

  • •Age < 18 years; pregnant or breastfeeding women
  • •TIMECARD score indicating mild risk
  • •Patients with terminal cancer or cancer for which active treatment has been declined
  • •Spontaneous hypothermia with a body temperature < 35°C; intracranial hemorrhage or massive bleeding
  • •Pre-arrest Cerebral Performance Category (CPC) score of 3-4; receipt of extracorporeal cardiopulmonary resuscitation (ECPR; CPR with ECMO)
  • •Refusal of participation by the patient's family

研究组 & 干预措施

Hypothermic PRN

Active Comparator

hypothermia + as needed

干预措施: Hypothermic (Procedure)

Hypothermic PRN

Active Comparator

hypothermia + as needed

干预措施: ASM as needed (Drug)

Hypothermic PPX

Experimental

hypothermia + Prophylactic treatment

干预措施: Prophylactic ASM (Drug)

Hypothermic PPX

Experimental

hypothermia + Prophylactic treatment

干预措施: Hypothermic (Procedure)

Normothermic PPX

Active Comparator

Normothermic + Prophylactic treatment

干预措施: Prophylactic ASM (Drug)

Normothermic PPX

Active Comparator

Normothermic + Prophylactic treatment

干预措施: Normothermic (Procedure)

Normothermic PRN

Active Comparator

Normothermic + as needed

干预措施: Normothermic (Procedure)

Normothermic PRN

Active Comparator

Normothermic + as needed

干预措施: ASM as needed (Drug)

结局指标

主要结局

clinical & electrical seizure occurrence

时间窗: Within 7 days after ROSC

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

National Taiwan University Clinical Trial Center

National Taiwan University Hospital

National Taiwan University Hospital

研究点 (1)

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