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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03261232
Other study ID # ELLOUZE 2016 Pro-ACR
Secondary ID
Status Active, not recruiting
Phase N/A
First received August 23, 2017
Last updated August 23, 2017
Start date March 2016
Est. completion date March 2018

Study information

Verified date August 2017
Source Centre Hospitalier Universitaire Dijon
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Through this retrospective observational study (over 4 years; period analysed: 1st January 2011 to 31st December 2014), we looked for prognostic factors associated with better survival in refractory cardiac arrest by:

- assessing the overall survival rate

- evaluating the frequency of intra et extra-hospital events and by comparing these with the survival rate

- studying no flow, low flow, rhythm at initial management, troponinemia, lactatemia and blood pH in the different groups.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 65
Est. completion date March 2018
Est. primary completion date March 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- Patients with in-hospital or out-of-hospital refractory CA who underwent ECLS

Exclusion Criteria:

- CA occurring during cardiac surgery

- Age > 75 years or < 18 years

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France CHU Dijon Bourgogne Dijon

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire Dijon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Survival rate at baseline
Primary Death rate at baseline
See also
  Status Clinical Trial Phase
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