Registry of cardiac arrest cases at Versailles Hospital
Official title: Versailles Hospital Cardiac Arrest Registry
Run by Versailles Hospital · NCT03594318 · Data updated 2026-11-12
This study collects information on patients who have cardiac arrest to see what factors affect their recovery and outcomes.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 1000 (estimated) |
| Sponsor | Versailles Hospital Academic / other |
| Locations | 1 site (Le Chesnay) |
| Status | Recruiting |
| Started | January 2006 |
| Main results expected | December 2026 |
| Study ends | December 2030 |
| Registry record updated | July 20, 2018 |
| Trial ID | NCT03594318 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults aged 18 and older who have experienced a cardiac arrest requiring intensive care.
✕Probably not a fit
Patients who refuse to participate in the study will not benefit from its findings.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
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.
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 gone: Other studies have successfully utilized similar observational approaches to improve understanding of cardiac arrest outcomes.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Cardiac arrest requiring Intensive Care Unit management * Age \>= 18 years Exclusion Criteria: \- Refusal to participate
Where it's running
-
CH Versailles
Le Chesnay, France Recruiting
Study contacts
- Study coordinator: Legriel Stephane, MD
- Email: slegriel@ch-versailles.fr
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Heartsight helps caregivers of kids after cardiac arrest manage uncertainty and fear
This pilot trial tests if the Heartsight information program is acceptable and helpful for caregivers of children who recently had a cardiac arrest.
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Cardiopulmonary resuscitation with balloon occlusion of the descending aorta for hospitalized patients
This trial will test whether adding a balloon occlusion of the descending aorta (REBOA) to standard ACLS helps people having an in-hospital cardiac arrest regain and keep a pulse.
-
Digital serious game to improve critical care nurses' targeted temperature management skills and situational awareness.
We will test whether adding a digital serious game to regular lectures helps adult ICU nurses learn targeted temperature management and improve situational awareness.
-
Plasma proteins, metabolites, and platelet changes in extracorporeal CPR for cardiac arrest patients
This project will test whether patterns in blood proteins, small molecules, and platelet shape changes can help identify which adults with cardiac arrest might benefit from extracorporeal CPR.
-
Targeted Temperature Management at 33°C for in-hospital cardiac arrest
This trial tests whether cooling patients who remain unconscious after a resuscitated in-hospital cardiac arrest to 33°C improves survival with good brain function compared to keeping a normal, controlled temperature.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.