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Early Neurological Assessment With Pupillometry in Cardiac Arrest During Resuscitation

NCT05192772 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 214

Last updated 2022-10-26

No results posted yet for this study

Summary

Easy Care study wants to demonstrate a correlation between intra-CPR infrared quantitative pupillometry and return of spontaneous circulation (ROSC).

Neurological pupil index (NPi) will be used alone and in association with end-tidal CO2.

Conditions

  • Cardiac Arrest
  • Out-Of-Hospital Cardiac Arrest

Interventions

DEVICE

NPi200

Digital pupillometry performed during cardiopulmonary resuscutation (CPR) every CPR cycle end in case of not intubated patient, or every 2 minutes in case of intubated patient

Sponsors & Collaborators

  • AREU - Agenzia Regionale Emergenza Urgenza

    collaborator UNKNOWN

  • Societa Italiana Anestesia Analgesia Rianimazione e Terapia Intensiva

    lead OTHER

Principal Investigators

  • Simone M Zerbi, MD · ASST Lariana Ospedale Sant'Anna di Como

  • Frank A Rasulo, Prof. · Division of Anesthesiology, Intensive Care & emergency Medicine, Università degli studi di Brescia

  • Marco Botteri, MD · AREU - Agenzia Regionale Emergenza Urgenza

  • Claudio Sandroni, Prof. · Institute of Anesthesiology and Intensive Care Medicine, Università Cattolica del Sacro Cuore, Roma.

  • Giovanni Chiarini, MD · Dip. Anestesia, Rianimazione ed Emergenze II, ASST Spedali Civili di Brescia

  • Maurizio Raimondi, MD · UOC Anestesia e Rianimazione Voghera e Oltrepò, ASST Pavia.

  • Antonio Bellasi, phD · Department of Medicine, Division of Nephrology, EOC, Lugano

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-12-01
Primary Completion
2023-07-01
Completion
2023-12-15

Countries

  • Italy

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05192772 on ClinicalTrials.gov