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Free Iron and Out of Hospital Cardiac Arrest (DESFER)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT03491670
Recruitment Status : Completed
First Posted : April 9, 2018
Last Update Posted : November 19, 2019
Sponsor:
Information provided by (Responsible Party):
University Hospital, Brest

Brief Summary:
Out of hospital cardiac arrest is associated with a poor prognosis. The aim of this study is to provide a better understanding of perturbations of iron metabolism after cardiac arrest and to analyze the impact on clinical centered outcome.

Condition or disease
Arrest Cardio Respiratory

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Study Type : Observational
Actual Enrollment : 25 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Iron Metabolism After Out of Hospital Cardiac Arrest
Actual Study Start Date : June 5, 2018
Actual Primary Completion Date : June 5, 2019
Actual Study Completion Date : July 16, 2019

Resource links provided by the National Library of Medicine





Primary Outcome Measures :
  1. Mortality [ Time Frame: through study completion, an average of 1 year ]
    Mortality


Secondary Outcome Measures :
  1. Neurologic outcome [ Time Frame: 6 months post cardiac arrest ]
    Cerebral Performance Categories scale, ranging from 1 to 5, with a patient considered "1" when he has good cerebral performance and 5 when he has very poor cerebral performance (including brain death)



Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients admitted to ICU for out of hospital cardiac arrest
Criteria

Inclusion Criteria:

  • Patient admitted to ICU for out of hospital cardiac arrest
  • Therapeutic hypothermia

Exclusion Criteria:

  • Absence of consent

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03491670


Locations
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France
CHRU de Brest
Brest, France, 29609
Sponsors and Collaborators
University Hospital, Brest

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Responsible Party: University Hospital, Brest
ClinicalTrials.gov Identifier: NCT03491670    
Other Study ID Numbers: DESFER (29BRC17.0154)
First Posted: April 9, 2018    Key Record Dates
Last Update Posted: November 19, 2019
Last Verified: November 2019

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Heart Arrest
Out-of-Hospital Cardiac Arrest
Heart Diseases
Cardiovascular Diseases