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Kinetics and Prognostic Value of NeuroFilament Light in Post-cardiac Arrest: A Prospective Multicenter Study

Kinetics and Prognostic Value of NeuroFilament Light in Post-cardiac Arrest: A Prospective Multicenter Study

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07760636
Acronym
CINEFIL
Enrollment
270
Registered
2026-08-12
Start date
2026-09-01
Completion date
2028-06-01
Last updated
2026-08-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Arrest (CA), Comatose, Intensive Care Unit (ICU) Admission, Return of Spontaneous Circulation

Keywords

Cardiac arrest, Coma, Neuroprognostication, Biomarkers, Neurofilament light chain

Brief summary

The purpose of this study is to assess the prognostic value of absolute value and kinetic of neurofilament light chain (NFL) collected at different time points (at admission, 12h, 24h, 48h, 72h, 96h, and day 7 after ICU admission) in predicting poor and good neurological outcome in comatose patients after cardiac arrest.

Detailed description

A large majority of patients resuscitated after cardiac arrest (CA) are comatose following the return of spontaneous circulation and require admission to the intensive care unit (ICU). Unfortunately, many of them die during their ICU stay, mainly following the decision to withdraw life-sustaining therapies due to ischemic and hypoxic brain injuries considered irreversible. Early identification of these neurological injury is therefore one of the major challenges for intensivists, in order to tailor the intensity of care. Currently, the recommended strategy consists of applying a multimodal prognostic approach. This algorithm allows prediction of poor neurological outcome in approximately 50% of cases, according to various studies. This highlights the need for new early prognostic markers to predict both unfavorable and favorable outcomes. Regarding biomarkers of brain injury, European guidelines recommend the measurement of serum NSE, a biomarker of neuronal injury that is now commonly used. An NSE level \> 60 µg/L at 48 and/or 72 hours after cardiac arrest predicts poor neurological outcome with good accuracy (AUC between 0.80 and 0.92 depending on the study), high specificity but limited sensitivity. Moreover, uncertainty remains regarding the optimal threshold value to use, and variable results have been reported across clinical studies. Finally, early serum NSE levels (within the first 24-48 hours) have limited prognostic value, which restricts their usefulness for the early identification of patients likely to have a poor outcome. These limitations have highlighted the need to identify new biomarkers of brain injury to better assess the prognosis of these patients.

Interventions

OTHERValue of neurofilament light chain (NFL) at different time points

Value of neurofilament light chain (NFL) at different time points (H0, H12, H24, H48, H72, H96, and day 7 after ICU admission

Sponsors

Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients admitted to the ICU for cardiac arrest, * Patients who regained consciousness following in-hospital or out-of-hospital cardiac arrest, * Patients in a coma upon arrival in the ICU, defined by a Glasgow Coma Scale (GCS) score \<8, * Patients included in the AfterROSC2 cohort,

Exclusion criteria

* Terminally ill patients (death expected within 3 hours of admission to the ICU), * Minors, * Patients under legal guardianship, * Pregnant women, * Patients not enrolled in a social security program, * Prior inclusion in the CINEFIL study, * Restriction of active therapies prior to the first NFL biomarker assay, * Objection by a family member or trusted person, if present

Design outcomes

Primary

MeasureTime frameDescription
modified Rankin Scale (mRS)3 monthsNeurological outcome assessed by the modified Rankin Scale (mRS) (An unfavorable outcome is defined as a modified Rankin Scale (mRS) score between 4 and 6 (severe neurological sequelae, persistent coma, or death), and a favorable outcome as a modified Rankin Scale (mRS) score between 0 and 3 (no sequelae, mild to moderate neurological sequelae))

Secondary

MeasureTime frameDescription
MortalityAt ICU discharge, up to 3 months
Early myoclonus<72 hoursClinical, imaging, or neurophysiological neurological abnormalities : early myoclonus (\<72 hours)
Myoclonus status<72 hours post-CAClinical, imaging, or neurophysiological neurological abnormalities: myoclonus status (\<72 hours post-CA)
Pupillary and corneal reflexes72 hours post-CAClinical, imaging, or neurophysiological neurological abnormalities: pupillary and corneal reflexes at 72 hours post-CA
Electroencephalogram (EEG)3 monthsNeurological abnormalities
Somatosensory evoked potentials3 monthsNeurological abnormalities
Auditory evoked potentials3 monthsNeurological abnormalities

Countries

France

Contacts

CONTACTSarah Benghanem, MD PhD
sarah.benghanem@aphp.fr+ 00 33 1 58 41 43 3
CONTACTMarie Benhammani-Godard
marie.godard@aphp.fr0033158411190
PRINCIPAL_INVESTIGATORSarah Benghanem

Medical ICU, Cochin hospital, Paris

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 13, 2026