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Not yet recruitingNCT07835802Updated Oct 7, 2026

The TTM and ASM Trial

A Phase 1 interventional study of Prophylactic ASM and Hypothermic in Critical Care Medicine, Emergency Medical Services and Cardiac Arrest (CA), sponsored by National Taiwan University Hospital. Not yet recruiting at 1 site in Taiwan. Open to participants aged 18 Years to 99 Years. Per ClinicalTrials.gov, last updated 2026-10-07.

Sponsored by National Taiwan University Hospital · Phase 1, Interventional, and Treatment

Phase
Phase 1
Study type
Interventional
Enrollment
100
Allocation
Randomized
Ages
18 Years to 99 Years
Sex
All
01

Study summary

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.

02

Conditions studied

  • Critical Care Medicine
  • Emergency Medical Services
  • Cardiac Arrest (CA)
  • Seizure

Keywords

  • Cardiac Arrest
  • Targeted Temperature Management
  • Seizure
  • Anti-Seizure Medication
  • outcome
03

In context

Heart Arrest

926 studies on the registry are indexed under Heart Arrest; 226 are open to participants now.

This study's planned enrollment of 100 is close to the median of 100 across 518 interventional studies indexed under Heart Arrest.

Browse Heart Arrest studies →

Lead sponsor

National Taiwan University Hospital is the lead sponsor of 2,615 studies on the registry; 576 are open to participants now.

Of its 11 completed or terminated interventional studies of FDA-regulated products, 2 (18%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 99 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

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

Exclusion criteria

Exclusion Criteria:

  1. Age \< 18 years; pregnant or breastfeeding women
  2. TIMECARD score indicating mild risk
  3. Patients with terminal cancer or cancer for which active treatment has been declined
  4. Spontaneous hypothermia with a body temperature \< 35°C; intracranial hemorrhage or massive bleeding
  5. Pre-arrest Cerebral Performance Category (CPC) score of 3-4; receipt of extracorporeal cardiopulmonary resuscitation (ECPR; CPR with ECMO)
  6. Refusal of participation by the patient's family
05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
100 participants (estimated)

Study arms

  • Experimental
    Hypothermic PPX

    hypothermia + Prophylactic treatment

    Drug: Prophylactic ASM · Procedure: Hypothermic

  • Active comparator
    Normothermic PPX

    Normothermic + Prophylactic treatment

    Drug: Prophylactic ASM · Procedure: Normothermic

  • Active comparator
    Hypothermic PRN

    hypothermia + as needed

    Procedure: Hypothermic · Drug: ASM as needed

  • Active comparator
    Normothermic PRN

    Normothermic + as needed

    Procedure: Normothermic · Drug: ASM as needed

Interventions

  • DrugProphylactic ASM

    Prophylactic treatment

  • ProcedureHypothermic

    TTM 33-34℃

  • ProcedureNormothermic

    TTM 36-37.5℃

  • DrugASM as needed

    as needed

06

What researchers measure

Primary outcomes

  1. clinical & electrical seizure occurrence

    Time frame: Within 7 days after ROSC

07

Study locations

1 site
08

References and documents

Study documents

PDFs hosted by the registry, ClinicalTrials.gov.

09

Updates

1 registry update since Sep 25, 2026
Minor edits
Nothing that changes what the study is or who can join. Edited: conditions
1 update, last Oct 7, 2026
Show all 1 update
  1. Oct 7, 2026
    Minor edits only
    + 1 other change: conditions

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07835802
Responsible party
National Taiwan University Clinical Trial Center (National Taiwan University Hospital, National Taiwan University Hospital) — Principal investigator
First posted
Sep 23, 2026
Start date
Sep 17, 2026 (estimated)
Primary completion
Jul 31, 2029 (estimated)
Completion
Jul 31, 2029 (estimated)
Last update
Oct 7, 2026

Study contacts

Min-Shan Tsai
Contact
mshanmshan@gmail.com
886-23123456 ext. 265632

Oversight

FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.

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