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Hypertonic LActaTe afTer cardiac arrEst: the LATTE trial

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2023-506031-15-01
Acronym
SRB2021260
Enrollment
125
Registered
2024-09-12
Start date
2025-02-18
Completion date
Unknown
Last updated
2024-10-18

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

Conditions

post-anoxic brain injury, Coma, Cardiac arrest, Post cardiac arrest syndrome

Brief summary

Neuron specific enolase (NSE) plasmatic peak values at 48 hours after return of spontaneous circulation.

Detailed description

Cerebral performance category score of 1 and 1-2 at 90 days., ICU length of stay (days), Hospital length of stay (days)., Mortality during ICU stay, during hospital stay, at 90 days., Vasopressor equivalent dose during the first 48h after resuscitation., Seizures episodes during the first 24h, 48h and ICU stay., Peak plasmatic concentrations or neurofilament light chain (NFL) at 24, 48 and 72h., Peak plasmatic concentrations or glial fibrillary acid protein (GFAP) at 24, 48 and 72h, Peak plasmatic concentrations or Troponin I (TnI) at 24, 48 and 72h, Incidence, nature, and severity of adverse events graded according to National Cancer Institute - Common Terminology Criteria for Adverse Events.

Interventions

DRUGsolution pour perfusion
DRUGSODIO LATTATO MONICO 2 mEq/ml concentrato per soluzione per infusione

Sponsors

Hopital Erasme
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Neuron specific enolase (NSE) plasmatic peak values at 48 hours after return of spontaneous circulation.

Secondary

MeasureTime frame
Cerebral performance category score of 1 and 1-2 at 90 days., ICU length of stay (days), Hospital length of stay (days)., Mortality during ICU stay, during hospital stay, at 90 days., Vasopressor equivalent dose during the first 48h after resuscitation., Seizures episodes during the first 24h, 48h and ICU stay., Peak plasmatic concentrations or neurofilament light chain (NFL) at 24, 48 and 72h., Peak plasmatic concentrations or glial fibrillary acid protein (GFAP) at 24, 48 and 72h, Peak plasmatic concentrations or Troponin I (TnI) at 24, 48 and 72h, Incidence, nature, and severity of adverse events graded according to National Cancer Institute - Common Terminology Criteria for Adverse Events.

Countries

Belgium

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026