Prehospital Cerebral Oxygenation During Cardiopulmonary Resuscitation (CPR)

This study has been completed.
Sponsor:
Collaborator:
Ziekenhuis Oost-Limburg
Information provided by (Responsible Party):
Cornelia Genbrugge, Hasselt University
ClinicalTrials.gov Identifier:
NCT01806844
First received: March 6, 2013
Last updated: April 19, 2016
Last verified: April 2016

March 6, 2013
April 19, 2016
May 2013
November 2015   (final data collection date for primary outcome measure)
prognostic value [ Time Frame: 1 year ] [ Designated as safety issue: No ]
Prognostic value of cerebral oxygenation during CPR
Same as current
Complete list of historical versions of study NCT01806844 on ClinicalTrials.gov Archive Site
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Prehospital Cerebral Oxygenation During Cardiopulmonary Resuscitation (CPR)
Cerebral Oxygenation During Resuscitation and Post-resuscitation Phase
Near infrared spectroscopy (NIRS) is a technique that measures regional cerebral oxygenation in a non-invasive manner. Through the use of near infrared light, the difference between oxygenated and deoxygenated hemoglobin can be measured. By applying the Beer-Lamber law, a numeric result can be calculated. During a cardiac arrest, there is no stroke volume, no cardiac output and no cerebral perfusion. By using cerebral NIRS during out-of hospital cardiac arrest, low flow time and return of spontaneous circulation, this study wants to show the prognostic value of NIRS as extra monitoring.
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Observational
Observational Model: Case-Only
Time Perspective: Prospective
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Non-Probability Sample
pre-hospital cardiac arrest
Cardiac Arrest
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Meex I, De Deyne C, Dens J, Scheyltjens S, Lathouwers K, Boer W, Vundelinckx G, Heylen R, Jans F. Feasibility of absolute cerebral tissue oxygen saturation during cardiopulmonary resuscitation. Crit Care. 2013 Mar 1;17(2):R36. doi: 10.1186/cc12546.

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
200
November 2015
November 2015   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • >16 year

Exclusion Criteria:

  • DNR code
Both
16 Years and older   (Child, Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
Belgium
 
NCT01806844
Copernicus I
No
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Cornelia Genbrugge, Hasselt University
Hasselt University
Ziekenhuis Oost-Limburg
Principal Investigator: Cornelia Genbrugge, MD Hasselt University
Hasselt University
April 2016

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP