Registry of cardiac arrest cases at Versailles Hospital
Versailles Hospital Cardiac Arrest Registry
This study collects information on patients who have cardiac arrest to see what factors affect their recovery and outcomes.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 1000 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Versailles Hospital Academic / other |
| Locations | 1 site (Le Chesnay) |
| Trial ID | NCT03594318 on ClinicalTrials.gov |
What this trial studies
This observational study collects data on patients who experience out-of-hospital and in-hospital cardiac arrest requiring intensive care unit management. It utilizes a standardized form to gather demographic information and details related to the cardiac arrest, following the Utstein guidelines. The study records the circumstances of the cardiac arrest, clinical findings, treatment timelines, and outcomes, including vital status and neurological performance at various follow-up points. The aim is to better understand the factors influencing outcomes in cardiac arrest patients.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older who have experienced a cardiac arrest requiring intensive care.
Not a fit: Patients who refuse to participate in the study will not benefit from its findings.
Why it matters
Potential benefit: If successful, this registry could improve understanding of cardiac arrest outcomes and inform better treatment protocols.
How similar studies have performed: Other studies have successfully utilized similar observational approaches to improve understanding of cardiac arrest outcomes.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Cardiac arrest requiring Intensive Care Unit management * Age \>= 18 years Exclusion Criteria: \- Refusal to participate
Where this trial is running
Le Chesnay
- CH Versailles — Le Chesnay, France (Recruiting)
Study contacts
- Study coordinator: Legriel Stephane, MD
- Email: slegriel@ch-versailles.fr
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.