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Recruiting NCT03594318

Versailles Hospital Cardiac Arrest Registry

Observational Cardiac Arrest

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Cardiac Arrest. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Out-of-hospital and in-hospital cardiac arrest (CA) requiring intensive care unit management. Data collection using a standardized form : demographic data and data related to the CA according to the Utstein guidelines.. Circumstances of onset, dates and times of onset and control of abnormal movements (myoclonus and.or seizures). On-scene clinical findings, pre-hospital and hospital care providers, timing of various treatments and supportive care, results of etiological investigations, cause of CA. Dates and times of EEG monitoring, EEG results. Outcomes including vital status and Cerebral Performance Category scale score at ICU and hospital discharge, day-90 and 1-year after CA and determined based on data in the ICU and/or hospital/neurologist charts and/or general practitionner phone interview.

Primary outcome measures

  • Long term favorable outcome [Time frame: 1 year]
Secondary outcome measures (5)
  • Short term favorable outcome [Time frame: 3 months]
  • Postanoxic Status Epilepticus [Time frame: 28 days]
  • Complications of anticoagulant/ antiplatelet therapies [Time frame: 28 days]
  • Short term quality of life as assessed by the Short Form (36) Health Survey (SF36) [Time frame: 3 months]
  • Long term quality of life as assessed by the Short Form (36) Health Survey (SF36) [Time frame: 1 year]

Eligibility criteria

Inclusion criteria

  • Cardiac arrest requiring Intensive Care Unit management
  • Age >= 18 years

Exclusion criteria

\- Refusal to participate

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

France · 1 center
  • CH Versailles — Le Chesnay

Identifiers

NCT: NCT03594318 · P13/20_ACR

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗